Allele Registry

Canonical Allele Identifier: PA121385

Gene: EMD HGNC NCBI

ClinVar RCV:

RCV000011926

RCV000078128

RCV002381248

ClinVar Variation:

11176

HGVS (amino-acid)	Matching Registered Transcripts
NP_000108.1:p.Gln44Ter