Canonical Allele Identifier: PA916023078
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49755
ClinVar RCV Id: RCV000043020 RCV000177445 RCV000565521 RCV000724630 RCV001086436
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Arg915Gln
CA019197
NM_001318831.2:c.2744G>A