Canonical Allele Identifier: PA2828413812
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230769

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Pro1221del
CA10579895
NM_001370404.1:c.3662_3664del