Canonical Allele Identifier: PA2827015708
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2626432
ClinVar RCV Id: RCV003382412

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ala1302Val
CA394304934
NM_001318831.2:c.3905C>T