Canonical Allele Identifier: PA891866382
Gene: SPTB HGNC NCBI

Linked Data

ClinVar Variation Id: 12841
ClinVar RCV Id: RCV000013693 RCV001000731 RCV001781258
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342366.1:p.Met1Val