Canonical Allele Identifier: PA891846633
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 583013
ClinVar RCV Id: RCV000707231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Asn828Ser
CA356912091
NM_000222.3:c.2483A>G