Canonical Allele Identifier: PA2827016162
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535873

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Pro1431Gln
CA394311256
NM_001318831.2:c.4292C>A