Allele Registry

Canonical Allele Identifier: PA2825102222

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000564380

RCV000628765

RCV002483539

RCV003237941

RCV003465263

ClinVar Variation:

485734

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Thr273Asn	CA4448034 NM_000245.4:c.818C>A