Allele Registry

Canonical Allele Identifier: PA2573163009

Gene: EMD HGNC NCBI

ClinVar RCV:

RCV001938533

ClinVar Variation:

1417656

HGVS (amino-acid)	Matching Registered Transcripts
NP_000108.1:p.Arg46Gln	CA337289104 NM_000117.3:c.137G>A