Canonical Allele Identifier: PA2827018470
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 664836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ser966Asn
CA043671
NM_001318832.2:c.2897G>A