Canonical Allele Identifier: PA2829019572
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 1061606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372217.1:p.Ser477Gly
CA356906367
NM_001385288.1:c.1429A>G