Canonical Allele Identifier: PA2827003737
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2075111
ClinVar RCV Id: RCV002963293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Met1156Ile
CA394292653
NM_001318827.2:c.3468G>A
CA394292655
NM_001318827.2:c.3468G>C
CA394292659
NM_001318827.2:c.3468G>T