Canonical Allele Identifier: PA2828415588
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Gln1708Glu
CA394314782
NM_001370404.1:c.5122C>G