Canonical Allele Identifier: PA2741823193
Gene: ERMN HGNC NCBI

Linked Data

ClinVar Variation Id: 2507869
ClinVar RCV Id: RCV004281633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001009959.1:p.Asp182Val
CA1917992
NM_001009959.3:c.545A>T