Canonical Allele Identifier: PA891866456
Gene: SPTB HGNC NCBI

Linked Data

ClinVar Variation Id: 313702
ClinVar RCV Id: RCV000349988 RCV000403325 RCV003137916
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342366.1:p.Arg2079His
CA7229718
NM_001355437.2:c.6236G>A