Allele Registry

Canonical Allele Identifier: PA176029

Gene: EMD HGNC NCBI

ClinVar RCV:

RCV000150648

RCV000638213

RCV001560049

RCV001831937

RCV002354342

ClinVar Variation:

163404

HGVS (amino-acid)	Matching Registered Transcripts
NP_000108.1:p.Trp200Arg	CA176027 NM_000117.3:c.598T>C CA415258982 NM_000117.3:c.598T>A