Canonical Allele Identifier: PA2828971088
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 13858
ClinVar RCV Id: RCV000014872

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372215.1:p.Arg791Gly
CA123527
NM_001385286.1:c.2371A>G