Canonical Allele Identifier: PA2828969021
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 161259

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372215.1:p.Ala178Thr
CA211566
NM_001385286.1:c.532G>A