Canonical Allele Identifier: PA2827015280
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ser1187Leu
CA050780
NM_001318831.2:c.3560C>T