Canonical Allele Identifier: PA264603
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Val1673Phe
CA021508
NM_000548.5:c.5017G>T