Canonical Allele Identifier: PA2825438303
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Asp1333Asn
CA319383
NM_001077183.3:c.3997G>A