Canonical Allele Identifier: PA2829021579
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 567141
ClinVar RCV Id: RCV000687137
ClinVar Variation Id: 576649

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372219.1:p.Val498Leu
CA356906532
NM_001385290.1:c.1492G>T
CA356906534
NM_001385290.1:c.1492G>C