Canonical Allele Identifier: PA2825439180
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 318335

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Asp1577Asn
CA053097
NM_001077183.3:c.4729G>A