Canonical Allele Identifier: PA2825573858
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467902
ClinVar RCV Id: RCV000532879
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Gln613His
CA394273020
NM_001114382.3:c.1839G>C
CA394273021
NM_001114382.3:c.1839G>T