Canonical Allele Identifier: PA2827015416
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406115

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Arg1226His
CA16614762
NM_001318831.2:c.3677G>A