Canonical Allele Identifier: PA645471917
Gene: EMD HGNC NCBI

Linked Data

ClinVar Variation Id: 425517
ClinVar RCV Id: RCV000487908 RCV002431424 RCV001865504
ClinVar Variation Id: 1351390
ClinVar RCV Id: RCV002044690
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000108.1:p.Gly28Arg
CA16621905
NM_000117.3:c.82G>A
CA415257191
NM_000117.3:c.82G>C