Canonical Allele Identifier: PA2826605734
Gene: ERMARD HGNC NCBI

Linked Data

ClinVar Variation Id: 507371
ClinVar RCV Id: RCV000605306 RCV000912441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265460.1:p.Glu2Val
CA4105683
NM_001278531.2:c.5A>T