Canonical Allele Identifier: PA2828093350
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 390104

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Pro1115Ala
CA046994
NM_001363528.2:c.3343C>G