Canonical Allele Identifier: PA2741959548
Gene: SOBP HGNC NCBI

Linked Data

ClinVar Variation Id: 2527817
ClinVar RCV Id: RCV004301081

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060483.3:p.Arg585Trp
CA365171217
NM_018013.4:c.1753C>T