Canonical Allele Identifier: PA170636
Gene: ELOVL5 HGNC NCBI

Linked Data

ClinVar Variation Id: 144075
ClinVar RCV Id: RCV000133587

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068586.1:p.Gly230Val
CA170635
NM_021814.5:c.689G>T