Canonical Allele Identifier: PA2828094860
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 318332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Asp1546Asn
CA10637331
NM_001363528.2:c.4636G>A