Canonical Allele Identifier: PA2828413079
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2564646
ClinVar RCV Id: RCV003297078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Gly1004Asp
CA394285202
NM_001370404.1:c.3011G>A