Canonical Allele Identifier: PA2827014265
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2564646
ClinVar RCV Id: RCV003297078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Gly804Asp
CA394285202
NM_001318831.2:c.2411G>A