Canonical Allele Identifier: PA2826059559
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1949560
ClinVar RCV Id: RCV002676309

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001162582.1:p.Arg13Ser
CA412194626
NM_001169111.2:c.39G>T
CA412194627
NM_001169111.2:c.39G>C