Canonical Allele Identifier: PA112050
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 13865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Val559Ala
CA123545
NM_000222.3:c.1676T>C