Canonical Allele Identifier: PA2828094375
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49925

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Asp1412His
CA020460
NM_001363528.2:c.4234G>C