Canonical Allele Identifier: PA916060988
Gene: SOBP HGNC NCBI

Linked Data

ClinVar Variation Id: 716742

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060483.3:p.Ser583Pro
CA3946576
NM_018013.4:c.1747T>C