Canonical Allele Identifier: PA2825573527
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3232082
ClinVar RCV Id: RCV004518797

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ser526Arg
CA394326663
NM_001114382.3:c.1576A>C
CA394326680
NM_001114382.3:c.1578C>A
CA394326682
NM_001114382.3:c.1578C>G