Allele Registry

Canonical Allele Identifier: PA2825619320

Gene: MET HGNC NCBI

ClinVar RCV:

RCV002391956

RCV003763152

ClinVar Variation:

1772394

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.His476Arg	CA368974069 NM_001127500.3:c.1427A>G