Canonical Allele Identifier: PA2827020136
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 639390
ClinVar RCV Id: RCV000792166 RCV004001563
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Gln1469Arg
CA394304325
NM_001318832.2:c.4406A>G