Allele Registry

Canonical Allele Identifier: PA188722

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000163595

RCV000167933

RCV000765920

RCV001293448

RCV001812140

RCV003398834

RCV003467280

ClinVar Variation:

184358

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Thr557Ala	CA188720 NM_001127500.3:c.1669A>G