Canonical Allele Identifier: PA2825436525
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 374680

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Arg786Cys
CA038725
NM_001077183.3:c.2356C>T