Canonical Allele Identifier: PA2827015348
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468084

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Arg1207Ser
CA050936
NM_001318831.2:c.3619C>A