Canonical Allele Identifier: PA2827005527
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535984

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Arg1646Gln
CA394314713
NM_001318827.2:c.4937G>A