Canonical Allele Identifier: PA2828418899
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2762661
ClinVar RCV Id: RCV003512525
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Pro903Leu
CA394279468
NM_001370405.1:c.2708C>T