Canonical Allele Identifier: PA645488367
Gene: KIT HGNC NCBI

Linked Data

ClinVar Variation Id: 409777
ClinVar RCV Id: RCV000463831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000213.1:p.Ser645Thr
CA16611604
NM_000222.3:c.1934G>C