Canonical Allele Identifier: PA155269
Gene: SOBP HGNC NCBI

Linked Data

ClinVar Variation Id: 130361
ClinVar RCV Id: RCV000118399 RCV001808344
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060483.3:p.Ser683Gly
CA155268
NM_018013.4:c.2047A>G