Canonical Allele Identifier: PA2825439408
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Leu1641Pro
CA021783
NM_001077183.3:c.4922T>C