Canonical Allele Identifier: PA2827019113
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3074520
ClinVar RCV Id: RCV004014054

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Trp1175Cys
CA394291543
NM_001318832.2:c.3525G>C
CA394291545
NM_001318832.2:c.3525G>T