Canonical Allele Identifier: PA2829948615
Gene: ERMN HGNC NCBI

Linked Data

ClinVar Variation Id: 2394103
ClinVar RCV Id: RCV004232601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065762.1:p.Asp191Gly
CA1917982
NM_020711.3:c.572A>G