Canonical Allele Identifier: PA2828414621
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ser1454Thr
CA020540
NM_001370404.1:c.4361G>C