Canonical Allele Identifier: PA2827015674
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Pro1294Ser
CA16615034
NM_001318831.2:c.3880C>T