Canonical Allele Identifier: PA2827007108
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 318313

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Pro492Arg
CA031797
NM_001318829.2:c.1475C>G