Allele Registry

Canonical Allele Identifier: PA645448255

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000425451

RCV000442904

RCV003168614

ClinVar Variation:

376126

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Met1268Thr	CA16602584 NM_001127500.3:c.3803T>C