Allele Registry

Canonical Allele Identifier: PA891866382

Gene: SPTB HGNC NCBI

ClinVar RCV:

RCV000013693

RCV001000731

RCV001781258

ClinVar Variation:

12841

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