Canonical Allele Identifier: PA2829979491
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1733615
ClinVar RCV Id: RCV002452497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Pro1175His
CA394291998
NM_021055.3:c.3524C>A