Canonical Allele Identifier: PA2825434963
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Leu309Phe
CA394315433
NM_001077183.3:c.925C>T