Canonical Allele Identifier: PA2829895271
Gene: SOBP HGNC NCBI

Linked Data

ClinVar Variation Id: 3167384
ClinVar RCV Id: RCV004464749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060483.3:p.Gly696Ser
CA365171910
NM_018013.4:c.2086G>A