Canonical Allele Identifier: PA324206
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 215128
ClinVar RCV Id: RCV001705133 RCV004020423
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005129.2:p.Ala176Val
CA324204
NM_005138.3:c.527C>T