Canonical Allele Identifier: PA2580129971
Gene: ERMN HGNC NCBI

Linked Data

ClinVar Variation Id: 2394103
ClinVar RCV Id: RCV004232601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001009959.1:p.Asp204Gly
CA1917982
NM_001009959.3:c.611A>G