Canonical Allele Identifier: PA2828417048
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_001357334.1:p.Thr374Ser
CA394319741
NM_001370405.1:c.1120A>T
CA394319747
NM_001370405.1:c.1121C>G