Canonical Allele Identifier: PA2825572827
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Tyr310Cys
CA10583288
NM_001114382.3:c.929A>G