Canonical Allele Identifier: PA2827011799
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1010404
ClinVar RCV Id: RCV001308024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Thr976Asn
CA394285777
NM_001318829.2:c.2927C>A