Canonical Allele Identifier: PA2826277690
Gene: ELOC HGNC NCBI

Linked Data

ClinVar Variation Id: 376557
ClinVar RCV Id: RCV000427598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191793.1:p.Tyr63Asn
CA16602983
NM_001204864.2:c.187T>A