Canonical Allele Identifier: PA2827013631
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49725
ClinVar RCV Id: RCV000042990 RCV000189999 RCV000201105
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Cys604Arg
CA017384
NM_001318831.2:c.1810T>C