Canonical Allele Identifier: PA2573086793
Gene: SCO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1311662
ClinVar RCV Id: RCV001752645
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005129.2:p.Met126Thr
CA10321220
NM_005138.3:c.377T>C