Canonical Allele Identifier: PA2573243822
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1374485
ClinVar RCV Id: RCV001883113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005129.2:p.Asp252Glu
CA10321116
NM_005138.3:c.756C>G
CA412190367
NM_005138.3:c.756C>A