Canonical Allele Identifier: PA2827016482
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Gln1508Glu
CA394314782
NM_001318831.2:c.4522C>G