Canonical Allele Identifier: PA2828410698
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Tyr310Cys
CA10583288
NM_001370404.1:c.929A>G