Canonical Allele Identifier: PA122741
Gene: SPTB HGNC NCBI

Linked Data

ClinVar Variation Id: 12837
ClinVar RCV Id: RCV000013688 RCV001004906 RCV002513020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020029.1:p.Ser2019Pro
CA122740
NM_001024858.4:c.6055T>C