Canonical Allele Identifier: PA2827015557
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535877

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ser1263Tyr
CA051496
NM_001318831.2:c.3788C>A