Canonical Allele Identifier: PA2573077730
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 41601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372213.1:p.Ala756Thr
CA215590
NM_001385284.1:c.2266G>A