Canonical Allele Identifier: PA2828094373
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Asp1412Asn
CA394302242
NM_001363528.2:c.4234G>A