Canonical Allele Identifier: PA2825438758
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_001070651.1:p.Gln1458Arg
CA394304325
NM_001077183.3:c.4373A>G