Canonical Allele Identifier: PA2827008413
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2564646
ClinVar RCV Id: RCV003297078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Gly956Asp
CA394285202
NM_001318829.2:c.2867G>A