Canonical Allele Identifier: PA645434354
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ser1449Phe
CA050898
NM_000548.5:c.4346C>T