Canonical Allele Identifier: PA2829981446
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Ser1455Thr
CA020540
NM_021055.3:c.4364G>C