Canonical Allele Identifier: PA2827004576
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Ser1395Thr
CA020540
NM_001318827.2:c.4184G>C