Canonical Allele Identifier: PA913199207
Gene: SPOP HGNC NCBI

Linked Data

ClinVar Variation Id: 376552
ClinVar RCV Id: RCV000432824 RCV000444738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001007229.1:p.Trp131Cys
CA16602978
NM_001007228.2:c.393G>T
CA400156698
NM_001007228.2:c.393G>C