Canonical Allele Identifier: PA645488161
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 409718

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Ser451Pro
CA2923476
NM_000222.3:c.1351T>C