Canonical Allele Identifier: PA2825576668
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ser1475Thr
CA020540
NM_001114382.3:c.4424G>C