Canonical Allele Identifier: PA2829023097
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 41601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372221.1:p.Ala751Thr
CA215590
NM_001385292.1:c.2251G>A