Canonical Allele Identifier: PA2828093719
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3064495
ClinVar RCV Id: RCV003989035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ser1226Cys
CA394293617
NM_001363528.2:c.3677C>G