Canonical Allele Identifier: PA2827013885
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1488823
ClinVar RCV Id: RCV001980328

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Asn682Lys
CA394279170
NM_001318831.2:c.2046T>A
CA394279172
NM_001318831.2:c.2046T>G