Canonical Allele Identifier: PA2828420684
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_001357334.1:p.Arg1434Ser
CA276753515
NM_001370405.1:c.4302G>C
CA394302236
NM_001370405.1:c.4302G>T