Canonical Allele Identifier: PA2829022789
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 1474017
ClinVar RCV Id: RCV001970981

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372221.1:p.Thr591Pro
CA356907827
NM_001385292.1:c.1771A>C