Canonical Allele Identifier: PA2825258479
Gene: ERLIN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 842326
ClinVar RCV Id: RCV001044725
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001003790.1:p.Met83del
CA916082982
NM_001003790.4:c.249_251del