Canonical Allele Identifier: PA2828413159
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3073959
ClinVar RCV Id: RCV004012501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Thr1031Pro
CA394285967
NM_001370404.1:c.3091A>C