Canonical Allele Identifier: PA2826277667
Gene: ELOC HGNC NCBI

Linked Data

ClinVar Variation Id: 376556
ClinVar RCV Id: RCV000443719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001191788.1:p.Tyr79Ser
CA16602982
NM_001204859.2:c.236A>C