Canonical Allele Identifier: PA2827020149
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 848503

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Glu1472Gln
CA394304419
NM_001318832.2:c.4414G>C