Canonical Allele Identifier: PA2580418568
Gene: SOBP HGNC NCBI

Linked Data

ClinVar Variation Id: 2239321
ClinVar RCV Id: RCV004105001
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060483.3:p.Asp596Glu
CA365171292
NM_018013.4:c.1788C>A
CA365171293
NM_018013.4:c.1788C>G