Canonical Allele Identifier: PA2828420383
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Glu1347Lys
CA050575
NM_001370405.1:c.4039G>A