Canonical Allele Identifier: PA2825092402
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 2625013
ClinVar RCV Id: RCV003377692
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Ala597Val
CA356907874
NM_000222.3:c.1790C>T