Canonical Allele Identifier: PA2828093906
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406054
ClinVar RCV Id: RCV000464141

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Gln1276Arg
CA16615150
NM_001363528.2:c.3827A>G