Canonical Allele Identifier: PA2826605751
Gene: ERMARD HGNC NCBI

Linked Data

ClinVar Variation Id: 386574
ClinVar RCV Id: RCV000432020 RCV000884634
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265460.1:p.Thr86Asn
CA4105777
NM_001278531.2:c.257C>A