Allele Registry

Canonical Allele Identifier: PA645471891

Gene: EMD HGNC NCBI

ClinVar Allele:

265324

ClinVar RCV:

RCV000518435

RCV001068392

ClinVar Variation:

281087

HGVS (amino-acid)	Matching Registered Transcripts
NP_000108.1:p.Met1Ile