Canonical Allele Identifier: PA2741959542
Gene: SOBP HGNC NCBI

Linked Data

ClinVar Variation Id: 2532993
ClinVar RCV Id: RCV004310295
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060483.3:p.Pro564Arg
CA365170956
NM_018013.4:c.1691C>G