Canonical Allele Identifier: PA2828412622
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237997
ClinVar RCV Id: RCV000234558 RCV002450675
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Asn859Thr
CA10583312
NM_001370404.1:c.2576A>C