Canonical Allele Identifier: PA2827021116
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 514715

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Gln1723Arg
CA055149
NM_001318832.2:c.5168A>G