Canonical Allele Identifier: PA645434400
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238046

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg1451His
CA050956
NM_000548.5:c.4352G>A