Canonical Allele Identifier: PA2828418079
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2102988
ClinVar RCV Id: RCV003019802

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Pro666Ala
CA394274424
NM_001370405.1:c.1996C>G