Canonical Allele Identifier: PA2828095366
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2847716
ClinVar RCV Id: RCV003628500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ala1676Gly
CA394314523
NM_001363528.2:c.5027C>G