Canonical Allele Identifier: PA645488167
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 409789

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Ala482Thr
CA16611597
NM_000222.3:c.1444G>A