Canonical Allele Identifier: PA2827008589
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 536003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Arg1035Gln
CA046441
NM_001318829.2:c.3104G>A