Canonical Allele Identifier: PA2827011996
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467845
ClinVar RCV Id: RCV000531383 RCV002438410 RCV003999245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Thr174Ser
CA394319741
NM_001318831.2:c.520A>T
CA394319747
NM_001318831.2:c.521C>G