Canonical Allele Identifier: PA2827016616
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2039590
ClinVar RCV Id: RCV002900008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ala1538Val
CA394315700
NM_001318831.2:c.4613C>T