Canonical Allele Identifier: PA916022829
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64897
ClinVar RCV Id: RCV000055098 RCV000491308
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Leu981Pro
CA018665
NM_001318827.2:c.2942T>C