Canonical Allele Identifier: PA2825092379
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 1779076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Asp579Val
CA356907597
NM_000222.3:c.1736A>T