Canonical Allele Identifier: PA2828415954
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 655432
ClinVar RCV Id: RCV000811607

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Thr41Ser
CA394301697
NM_001370405.1:c.121A>T
CA394301701
NM_001370405.1:c.122C>G