Canonical Allele Identifier: PA645448119
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 246635
ClinVar RCV Id: RCV001306836
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Leu973Gln
CA10584665
NM_001127500.3:c.2918T>A