Canonical Allele Identifier: PA2825434775
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 318307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ile247Val
CA056277
NM_001077183.3:c.739A>G