Allele Registry

Canonical Allele Identifier: PA2825618990

Gene: MET HGNC NCBI

ClinVar RCV:

RCV002025609

RCV003303620

RCV003442995

ClinVar Variation:

1503654

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.His396Pro	CA368970737 NM_001127500.3:c.1187A>C