Canonical Allele Identifier: PA2829948613
Gene: ERMN HGNC NCBI

Linked Data

ClinVar Variation Id: 2507869
ClinVar RCV Id: RCV004281633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065762.1:p.Asp169Val
CA1917992
NM_020711.3:c.506A>T