Canonical Allele Identifier: PA2825577628
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 574061
ClinVar RCV Id: RCV000695896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Arg1728Pro
CA394314761
NM_001114382.3:c.5183G>C