Canonical Allele Identifier: PA2827009841
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49486
ClinVar Variation Id: 65278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Gln1439His
CA020854
NM_001318829.2:c.4317G>C
CA020857
NM_001318829.2:c.4317G>T