Canonical Allele Identifier: PA2828965729
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 1771653
ClinVar RCV Id: RCV002389130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372214.1:p.Gly466Trp
CA356906309
NM_001385285.1:c.1396G>T