Canonical Allele Identifier: PA2828412761
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1516394

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Pro903Thr
CA394279461
NM_001370404.1:c.2707C>A