Canonical Allele Identifier: PA335179
Gene: EMD HGNC NCBI

Linked Data

ClinVar Variation Id: 201783
ClinVar RCV Id: RCV000726925 RCV001827990 RCV002415780 RCV001420800 RCV001852357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000108.1:p.Asp72Val
CA335177
NM_000117.3:c.215A>T