Canonical Allele Identifier: PA2580326956
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1949560
ClinVar RCV Id: RCV002676309

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005129.2:p.Arg13Ser
CA412194626
NM_005138.3:c.39G>T
CA412194627
NM_005138.3:c.39G>C