Canonical Allele Identifier: PA2827009553
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535938

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Pro1353Leu
CA051050
NM_001318829.2:c.4058C>T