Canonical Allele Identifier: PA2827002649
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64921

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Leu807Pro
CA017563
NM_001318827.2:c.2420T>C