Canonical Allele Identifier: PA2580387354
Gene: SBDS HGNC NCBI

Linked Data

ClinVar Variation Id: 1794536
ClinVar RCV Id: RCV002428795
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057122.2:p.Thr89Ser
CA4279191
NM_016038.2:c.266C>G
CA367650874
NM_016038.2:c.265A>T