Canonical Allele Identifier: PA262605
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49350
ClinVar RCV Id: RCV000042610 RCV000517378
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Pro1709Arg
CA021789
NM_000548.5:c.5126C>G