Canonical Allele Identifier: PA2827016424
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 825547

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Pro1493Ala
CA394314331
NM_001318831.2:c.4477C>G