Canonical Allele Identifier: PA2828050287
Gene: SPTB HGNC NCBI

Linked Data

ClinVar Variation Id: 313723
ClinVar RCV Id: RCV000283035 RCV000375251 RCV003546516 RCV003338569 RCV003910181
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342365.1:p.Pro1613Ser
CA7230185
NM_001355436.2:c.4837C>T