Canonical Allele Identifier: PA2827015210
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Arg1165Gly
CA276753368
NM_001318831.2:c.3493C>G