Canonical Allele Identifier: PA2827014299
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2747514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Leu817Met
CA394285548
NM_001318831.2:c.2449C>A