Canonical Allele Identifier: PA2825577618
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535984

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Arg1726Gln
CA394314713
NM_001114382.3:c.5177G>A