Canonical Allele Identifier: PA2825438815
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2633616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Asp1474Gly
CA394304815
NM_001077183.3:c.4421A>G