Canonical Allele Identifier: PA2829948617
Gene: ERMN HGNC NCBI

Linked Data

ClinVar Variation Id: 2532970
ClinVar RCV Id: RCV004310279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065762.1:p.Asp197Gly
CA348667762
NM_020711.3:c.590A>G