Canonical Allele Identifier: PA2825436709
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Leu850Pro
CA017661
NM_001077183.3:c.2549T>C