Canonical Allele Identifier: PA2580231728
Gene: SPTB HGNC NCBI

Linked Data

ClinVar Variation Id: 2225104
ClinVar RCV Id: RCV002683725
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342366.1:p.Glu1755Lys
CA262689334
NM_001355437.2:c.5263G>A