Canonical Allele Identifier: PA2827009372
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2827102
ClinVar RCV Id: RCV003628133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ser1296Arg
CA394300235
NM_001318829.2:c.3886A>C
CA394300264
NM_001318829.2:c.3888C>A
CA394300268
NM_001318829.2:c.3888C>G