Canonical Allele Identifier: PA2829019734
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 222957
ClinVar RCV Id: RCV000208566
ClinVar Variation Id: 627639
ClinVar RCV Id: RCV000771010

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372217.1:p.Trp554_Lys555del
CA356974
NM_001385288.1:c.1660_1665del
CA645516812
NM_001385288.1:c.1659_1664delinsACCTTC
CA645516823
NM_001385288.1:c.1660_1663delinsG
CA645516826
NM_001385288.1:c.1661_1665delinsTTCCT
CA645516828
NM_001385288.1:c.1661_1664delinsCTTC
CA645516830
NM_001385288.1:c.1662_1665delinsC
CA645516831
NM_001385288.1:c.1662_1664delinsCAC
CA645516832
NM_001385288.1:c.1662_1664delinsTCC
CA913189821
NM_001385288.1:c.1656_1663delinsCC