Canonical Allele Identifier: PA2829019269
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 161260

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372217.1:p.Met319Val
CA211569
NM_001385288.1:c.955A>G