Canonical Allele Identifier: PA2828090114
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Asp162Asn
CA394309028
NM_001363528.2:c.484G>A