Canonical Allele Identifier: PA2828091320
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Arg537His
CA031730
NM_001363528.2:c.1610G>A