Canonical Allele Identifier: PA2825576287
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 380381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Pro1366Ser
CA16607165
NM_001114382.3:c.4096C>T