Canonical Allele Identifier: PA2826889383
Gene: ERMN HGNC NCBI

Linked Data

ClinVar Variation Id: 2532970
ClinVar RCV Id: RCV004310279
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291273.1:p.Asp197Gly
CA348667762
NM_001304344.2:c.590A>G