Canonical Allele Identifier: PA2828413696
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406092
ClinVar RCV Id: RCV000475309 RCV002348295
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Gln1185Arg
CA16614724
NM_001370404.1:c.3554A>G