Canonical Allele Identifier: PA2827019727
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2827102
ClinVar RCV Id: RCV003628133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ser1355Arg
CA394300235
NM_001318832.2:c.4063A>C
CA394300264
NM_001318832.2:c.4065C>A
CA394300268
NM_001318832.2:c.4065C>G