Canonical Allele Identifier: PA658805110
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535984

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg1749Gln
CA394314713
NM_000548.5:c.5246G>A