Allele Registry

Canonical Allele Identifier: PA2825620277

Gene: MET HGNC NCBI

ClinVar RCV:

RCV002041269

ClinVar Variation:

1518101

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Glu740Asp	CA368980769 NM_001127500.3:c.2220A>C CA368980771 NM_001127500.3:c.2220A>T