Canonical Allele Identifier: PA2826605961
Gene: ERMARD HGNC NCBI

Linked Data

ClinVar Variation Id: 380785
ClinVar RCV Id: RCV000437289 RCV001420687 RCV002062351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265461.1:p.Arg376His
CA4106290
NM_001278532.2:c.1127G>A