Canonical Allele Identifier: PA2825439502
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468145

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Asn1664Lys
CA394314174
NM_001077183.3:c.4992C>A
CA394314180
NM_001077183.3:c.4992C>G