Canonical Allele Identifier: PA2827016508
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406083

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Glu1513Lys
CA16615048
NM_001318831.2:c.4537G>A