Canonical Allele Identifier: PA916023619
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65084

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Arg596His
CA015651
NM_001318832.2:c.1787G>A