Canonical Allele Identifier: PA2825573578
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 318313

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Pro541Arg
CA031797
NM_001114382.3:c.1622C>G