Canonical Allele Identifier: PA915966298
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 438769
ClinVar RCV Id: RCV000505599

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Asp952Ter
CA645509146
NM_000222.3:c.2851_2852dup