Canonical Allele Identifier: PA2826889420
Gene: ERMN HGNC NCBI

Linked Data

ClinVar Variation Id: 2507869
ClinVar RCV Id: RCV004281633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291275.1:p.Asp149Val
CA1917992
NM_001304346.2:c.446A>T