Canonical Allele Identifier: PA2573088290
Gene: ERLIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1344327

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006450.2:p.Tyr298Cys
CA5645963
NM_006459.4:c.893A>G