Canonical Allele Identifier: PA658672861
Gene: EMD HGNC NCBI

Linked Data

ClinVar Variation Id: 462827
ClinVar RCV Id: RCV000618581 RCV000762691 RCV000551537 RCV001829576
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000108.1:p.Arg204His
CA10561647
NM_000117.3:c.611G>A