Canonical Allele Identifier: PA293440
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 139082
ClinVar Variation Id: 2885252
ClinVar RCV Id: RCV003717163

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005129.2:p.Arg20Pro
CA293438
NM_005138.3:c.59G>C
CA2739268037
NM_005138.3:c.59_60delinsCA