Canonical Allele Identifier: PA2827015342
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468083

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Pro1206Ala
CA050903
NM_001318831.2:c.3616C>G