Canonical Allele Identifier: PA2828093723
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1735113
ClinVar RCV Id: RCV002355213 RCV003102451
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Asn1227His
CA394293629
NM_001363528.2:c.3679A>C