Canonical Allele Identifier: PA2829022709
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 13856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372221.1:p.Val556Asp
CA123522
NM_001385292.1:c.1667T>A