Canonical Allele Identifier: PA2828970321
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 375919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372215.1:p.Leu572Pro
CA16602401
NM_001385286.1:c.1715T>C
CA891841855
NM_001385286.1:c.1715_1719delinsCTCCC