Canonical Allele Identifier: PA2573161507
Gene: EMD HGNC NCBI

Linked Data

ClinVar Variation Id: 1491927
ClinVar RCV Id: RCV002010192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000108.1:p.Arg211Gly
CA415259057
NM_000117.3:c.631C>G