Canonical Allele Identifier: PA2828414785
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2633616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Asp1497Gly
CA394304815
NM_001370404.1:c.4490A>G