Canonical Allele Identifier: PA2828419071
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 649255

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ser956Thr
CA394283753
NM_001370405.1:c.2867G>C