Canonical Allele Identifier: PA319451
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207718

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Glu532Lys
CA319449
NM_000548.5:c.1594G>A