Canonical Allele Identifier: PA2825437173
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2564646
ClinVar RCV Id: RCV003297078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Gly1004Asp
CA394285202
NM_001077183.3:c.3011G>A