Canonical Allele Identifier: PA2828967068
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 41601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372214.1:p.Ala754Thr
CA215590
NM_001385285.1:c.2260G>A