Canonical Allele Identifier: PA2825187610
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1741992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.His1543Gln
CA051970
NM_000548.5:c.4629C>G
CA394304854
NM_000548.5:c.4629C>A