Canonical Allele Identifier: PA2826889424
Gene: ERMN HGNC NCBI

Linked Data

ClinVar Variation Id: 2532970
ClinVar RCV Id: RCV004310279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291275.1:p.Asp177Gly
CA348667762
NM_001304346.2:c.530A>G