Canonical Allele Identifier: PA2828094376
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 641928
ClinVar RCV Id: RCV000795284

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Asp1412Val
CA394302256
NM_001363528.2:c.4235A>T