Canonical Allele Identifier: PA2827415969
Gene: ERLIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1344327
ClinVar RCV Id: RCV001848430 RCV004038701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334785.1:p.Tyr214Cys
CA5645963
NM_001347856.2:c.641A>G