Canonical Allele Identifier: PA891866453
Gene: SPTB HGNC NCBI

Linked Data

ClinVar Variation Id: 522602
ClinVar RCV Id: RCV000625738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342366.1:p.Leu2032Pro
CA390039437
NM_001355437.2:c.6095T>C