Canonical Allele Identifier: PA155267
Gene: SOBP HGNC NCBI

Linked Data

ClinVar Variation Id: 130360
ClinVar RCV Id: RCV000118398 RCV000427101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060483.3:p.Ile539Val
CA155266
NM_018013.4:c.1615A>G