Canonical Allele Identifier: PA2827020996
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Gln1696Glu
CA394314782
NM_001318832.2:c.5086C>G