Canonical Allele Identifier: PA2827416253
Gene: ERLIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1512511
ClinVar RCV Id: RCV002045669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334790.1:p.Lys151Glu
CA378154504
NM_001347861.2:c.451A>G