Canonical Allele Identifier: PA2829020214
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 13858
ClinVar RCV Id: RCV000014872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001372217.1:p.Arg793Gly
CA123527
NM_001385288.1:c.2377A>G