Allele Registry

Canonical Allele Identifier: PA2573200774

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001878703

ClinVar Variation:

1370848

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Pro583Arg	CA368987773 NM_001324402.2:c.1748C>G