Canonical Allele Identifier: PA916027566
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 13886
ClinVar RCV Id: RCV000014900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Leu765Val
CA257006
NM_001324402.2:c.2293C>G