Canonical Allele Identifier: PA2827008877
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2016405
ClinVar RCV Id: RCV002843884

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Gln1137His
CA394292399
NM_001318829.2:c.3411G>C
CA394292405
NM_001318829.2:c.3411G>T