Allele Registry

Canonical Allele Identifier: PA2827253862

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000163595

RCV000167933

RCV000765920

RCV001293448

RCV001812140

RCV003398834

RCV003467280

ClinVar Variation:

184358

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Thr127Ala	CA188720 NM_001324402.2:c.379A>G