Canonical Allele Identifier: PA915971222
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 41606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001087241.1:p.Thr304Ala
CA215605
NM_001093772.2:c.910A>G