Canonical Allele Identifier: PA2828421731
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406110
ClinVar RCV Id: RCV000471307 RCV004022585
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Glu1710Asp
CA16614803
NM_001370405.1:c.5130A>C
CA394315121
NM_001370405.1:c.5130A>T