Canonical Allele Identifier: PA2828050518
Gene: SPTB HGNC NCBI

Linked Data

ClinVar Variation Id: 996355
ClinVar RCV Id: RCV001290762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342365.1:p.Thr2058Met
CA7229750
NM_001355436.2:c.6173C>T