Canonical Allele Identifier: PA2741823195
Gene: ERMN HGNC NCBI

Linked Data

ClinVar Variation Id: 2532970
ClinVar RCV Id: RCV004310279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001009959.1:p.Asp210Gly
CA348667762
NM_001009959.3:c.629A>G