Canonical Allele Identifier: PA2827009483
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ser1334Phe
CA050898
NM_001318829.2:c.4001C>T