Canonical Allele Identifier: PA264546
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65074
ClinVar RCV Id: RCV000055281 RCV001853092
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ala889Pro
CA017834
NM_000548.5:c.2665G>C