Canonical Allele Identifier: PA2827015320
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Pro1200Ala
CA394301394
NM_001318831.2:c.3598C>G