Allele Registry

Canonical Allele Identifier: PA891866387

Gene: SPTB HGNC NCBI

ClinVar RCV:

RCV000655908

RCV003133483

RCV003432719

ClinVar Variation:

544811

HGVS (amino-acid)	Matching Registered Transcripts
NP_001342366.1:p.Arg216Gln	CA390031881 NM_001355437.2:c.647G>A