Canonical Allele Identifier: PA915976212
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405954
ClinVar RCV Id: RCV000462321 RCV002311770 RCV004000677
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Arg976Trp
CA042810
NM_001114382.3:c.2926C>T