Allele Registry

Canonical Allele Identifier: PA325736

Gene: EMD HGNC NCBI

ClinVar Allele:

44694

ClinVar RCV:

RCV000686102

RCV003103716

RCV003492301

ClinVar Variation:

36030

HGVS (amino-acid)	Matching Registered Transcripts
NP_000108.1:p.Arg157Gln	CA325734 NM_000117.3:c.470G>A