Canonical Allele Identifier: PA2825439587
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207760

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Arg1684His
CA054581
NM_001077183.3:c.5051G>A