Canonical Allele Identifier: PA2828419812
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1733712
ClinVar RCV Id: RCV002452586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Asp1179Tyr
CA394292119
NM_001370405.1:c.3535G>T