Canonical Allele Identifier: PA658804569
Gene: EMD HGNC NCBI

Linked Data

ClinVar Variation Id: 531735
ClinVar RCV Id: RCV000638220

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000108.1:p.Gly28Glu
CA415257262
NM_000117.3:c.83G>A