Allele Registry

Canonical Allele Identifier: PA2825619238

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001237256

ClinVar Variation:

963255

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Gly456Arg	CA368973062 NM_001127500.3:c.1366G>A CA368973064 NM_001127500.3:c.1366G>C