Canonical Allele Identifier: PA915990607
Gene: SPOP HGNC NCBI

Linked Data

ClinVar Variation Id: 376552
ClinVar RCV Id: RCV000432824 RCV000444738
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003554.1:p.Trp131Cys
CA16602978
NM_003563.3:c.393G>T
CA400156698
NM_003563.3:c.393G>C