Canonical Allele Identifier: PA131138
Gene: EMD HGNC NCBI

Linked Data

ClinVar Variation Id: 42278
ClinVar RCV Id: RCV000035111 RCV001089148 RCV002354186 RCV000732781
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000108.1:p.Gly216Arg
CA131136
NM_000117.3:c.646G>A
CA415259086
NM_000117.3:c.646G>C