Canonical Allele Identifier: PA2827254694
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 411908
ClinVar RCV Id: RCV000470541 RCV001018162 RCV002291639 RCV001837917
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Thr562Ala
CA4448620
NM_001324402.2:c.1684A>G