Canonical Allele Identifier: PA257008
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_001120972.1:p.Leu1213Val
CA257006
NM_001127500.3:c.3637C>G