Canonical Allele Identifier: PA2741809538
Gene: EMD HGNC NCBI

Linked Data

ClinVar Variation Id: 2758175
ClinVar RCV Id: RCV003524656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000108.1:p.Arg31Pro
CA415257303
NM_000117.3:c.92G>C