Canonical Allele Identifier: PA160352
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 134621

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Val530Ile
CA160350
NM_000222.3:c.1588G>A