Canonical Allele Identifier: PA2827016462
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1517318
ClinVar RCV Id: RCV002027265

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ile1503Phe
CA394314631
NM_001318831.2:c.4507A>T