Canonical Allele Identifier: PA2828418100
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1399324
ClinVar RCV Id: RCV001893773 RCV002423000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Gly671Ser
CA394274467
NM_001370405.1:c.2011G>A