Allele Registry

Canonical Allele Identifier: PA102500

Gene: EMD HGNC NCBI

ClinVar RCV:

RCV000011929

ClinVar Variation:

11179

HGVS (amino-acid)	Matching Registered Transcripts
NP_000108.1:p.Pro183Thr	CA121389 NM_000117.3:c.547C>A