Canonical Allele Identifier: PA891866386
Gene: SPTB HGNC NCBI

Linked Data

ClinVar Variation Id: 12835
ClinVar RCV Id: RCV000013684
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342366.1:p.Trp202Arg
CA122736
NM_001355437.2:c.604T>C
CA390032073
NM_001355437.2:c.604T>A