Canonical Allele Identifier: PA2827020340
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49956

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Gly1523Ser
CA020963
NM_001318832.2:c.4567G>A