Canonical Allele Identifier: PA2825438780
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1398100

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Val1464Met
CA051890
NM_001077183.3:c.4390G>A