Canonical Allele Identifier: PA2827014725
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65034

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Arg1024His
CA019556
NM_001318831.2:c.3071G>A