Canonical Allele Identifier: PA916022816
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 571585
ClinVar RCV Id: RCV000692769 RCV002325386
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Ser965Cys
CA394285144
NM_001318827.2:c.2894C>G