Canonical Allele Identifier: PA2827416287
Gene: ERLIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1344327

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334790.1:p.Tyr298Cys
CA5645963
NM_001347861.2:c.893A>G