Allele Registry

Canonical Allele Identifier: PA658669284

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000564380

RCV000628765

RCV002483539

RCV003237941

RCV003465263

ClinVar Variation:

485734

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Thr273Asn	CA4448034 NM_001127500.3:c.818C>A