Canonical Allele Identifier: PA2829974608
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 379559
ClinVar RCV Id: RCV000546851 RCV000444052 RCV002411311 RCV000767144
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Gly630Asp
CA16606929
NM_021055.3:c.1889G>A