Canonical Allele Identifier: PA2827016395
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468145

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Asn1487Lys
CA394314174
NM_001318831.2:c.4461C>A
CA394314180
NM_001318831.2:c.4461C>G