Canonical Allele Identifier: PA2829979654
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406101
ClinVar RCV Id: RCV000460265 RCV002365619
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Thr1204Ala
CA048226
NM_021055.3:c.3610A>G