Canonical Allele Identifier: PA1139724883
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 902939
ClinVar RCV Id: RCV001149866 RCV001149867 RCV001882460 RCV003405357
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005129.2:p.Val181Ile
CA10321175
NM_005138.3:c.541G>A