Canonical Allele Identifier: PA891866378
Gene: SPTB HGNC NCBI

Linked Data

ClinVar Variation Id: 257135
ClinVar RCV Id: RCV000242243
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342365.1:p.Ser2161Arg
CA7229555
NM_001355436.2:c.6483C>A
CA390037008
NM_001355436.2:c.6483C>G
CA390037013
NM_001355436.2:c.6481A>C