Canonical Allele Identifier: PA215601
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 41604

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Thr274Met
CA215599
NM_000222.3:c.821C>T