Canonical Allele Identifier: PA2828411607
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65084

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Arg585His
CA015651
NM_001370404.1:c.1754G>A