Canonical Allele Identifier: PA2825436688
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64921

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Leu844Pro
CA017563
NM_001077183.3:c.2531T>C