Canonical Allele Identifier: PA2825435901
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 41730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ala607Thr
CA015854
NM_001077183.3:c.1819G>A