Canonical Allele Identifier: PA2828412785
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1795250
ClinVar RCV Id: RCV002431341

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Pro910Ile
CA2580090869
NM_001370404.1:c.2728_2729delinsAT