Allele Registry

Canonical Allele Identifier: PA658803603

Gene: MET HGNC NCBI

ClinVar Allele:

522773

ClinVar RCV:

RCV000628769

RCV000765921

RCV001021839

RCV001766335

RCV002268220

RCV003459489

ClinVar Variation:

524889

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Ile1363Thr	CA4448820 NM_001127500.3:c.4088T>C