Canonical Allele Identifier: PA2828094043
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Pro1315Leu
CA020000
NM_001363528.2:c.3944C>T