Allele Registry

Canonical Allele Identifier: PA2827254207

Gene: MET HGNC NCBI

ClinVar RCV:

RCV002041269

ClinVar Variation:

1518101

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Glu310Asp	CA368980769 NM_001324402.2:c.930A>C CA368980771 NM_001324402.2:c.930A>T