Canonical Allele Identifier: PA2825439570
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1517318
ClinVar RCV Id: RCV002027265

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ile1680Phe
CA394314631
NM_001077183.3:c.5038A>T