Canonical Allele Identifier: PA2827014604
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1733712
ClinVar RCV Id: RCV002452586

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Asp978Tyr
CA394292119
NM_001318831.2:c.2932G>T