Canonical Allele Identifier: PA2828414545
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 642802
ClinVar RCV Id: RCV000796334
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Arg1433Ser
CA276753515
NM_001370404.1:c.4299G>C
CA394302236
NM_001370404.1:c.4299G>T