Canonical Allele Identifier: PA916022906
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406031
ClinVar RCV Id: RCV000458732 RCV002365618
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Pro32Ser
CA056156
NM_001318831.2:c.94C>T