Allele Registry

Canonical Allele Identifier: PA2580104288

Gene: EMD HGNC NCBI

ClinVar RCV:

RCV002781024

ClinVar Variation:

1985808

HGVS (amino-acid)	Matching Registered Transcripts
NP_000108.1:p.Arg47Trp	CA415257473 NM_000117.3:c.139C>T