Canonical Allele Identifier: PA2825571951
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1043681
ClinVar RCV Id: RCV001347824 RCV002368143
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Thr41Ile
CA394301702
NM_001114382.3:c.122C>T