Canonical Allele Identifier: PA2825572323
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.His152Asp
CA020642
NM_001114382.3:c.454C>G