Canonical Allele Identifier: PA645435167
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 265281

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Glu1583Lys
CA10588598
NM_000548.5:c.4747G>A