Canonical Allele Identifier: PA2825434378
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468016

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Arg115His
CA046888
NM_001077183.3:c.344G>A