Canonical Allele Identifier: PA2827005370
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49931

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Arg1610Pro
CA021846
NM_001318827.2:c.4829G>C