Canonical Allele Identifier: PA2828963010
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 1771653
ClinVar RCV Id: RCV002389130

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372213.1:p.Gly467Trp
CA356906309
NM_001385284.1:c.1399G>T