Allele Registry

Canonical Allele Identifier: PA645472180

Gene: EMD HGNC NCBI

ClinVar RCV:

RCV000725843

RCV001088437

RCV003492028

ClinVar Variation:

286452

HGVS (amino-acid)	Matching Registered Transcripts
NP_000108.1:p.Arg204Gly	CA10561646 NM_000117.3:c.610C>G