Canonical Allele Identifier: PA2829020141
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 41601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372217.1:p.Ala752Thr
CA215590
NM_001385288.1:c.2254G>A