Canonical Allele Identifier: PA2825439547
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2847716
ClinVar RCV Id: RCV003628500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ala1675Gly
CA394314523
NM_001077183.3:c.5024C>G