Canonical Allele Identifier: PA2827015651
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1398100

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Val1287Met
CA051890
NM_001318831.2:c.3859G>A