Allele Registry

Canonical Allele Identifier: PA645471917

Gene: EMD HGNC NCBI

ClinVar RCV:

RCV000487908

RCV001865504

RCV002044690

RCV002431424

ClinVar Variation:

425517

1351390

HGVS (amino-acid)	Matching Registered Transcripts
NP_000108.1:p.Gly28Arg	CA16621905 NM_000117.3:c.82G>A CA415257191 NM_000117.3:c.82G>C