Canonical Allele Identifier: PA2825577609
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1517318
ClinVar RCV Id: RCV002027265

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ile1724Phe
CA394314631
NM_001114382.3:c.5170A>T