Canonical Allele Identifier: PA2829022776
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 1779283
ClinVar RCV Id: RCV002401482

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372221.1:p.Trp579Leu
CA356907621
NM_001385292.1:c.1736G>T