Canonical Allele Identifier: PA2829018601
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 1430082
ClinVar RCV Id: RCV001931323
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372215.1:p.Val847Ala
CA2923792
NM_001385286.1:c.2540T>C