Canonical Allele Identifier: PA2827017177
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468174

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Asn240Ser
CA394312549
NM_001318832.2:c.719A>G