Canonical Allele Identifier: PA2829022731
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 41600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372221.1:p.Gly562Val
CA215587
NM_001385292.1:c.1685G>T