Canonical Allele Identifier: PA2826277693
Gene: ELOC HGNC NCBI

Linked Data

ClinVar Variation Id: 376556
ClinVar RCV Id: RCV000443719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191793.1:p.Tyr63Ser
CA16602982
NM_001204864.2:c.188A>C