Canonical Allele Identifier: PA2825574746
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Asn859Thr
CA10583312
NM_001114382.3:c.2576A>C