Canonical Allele Identifier: PA2829970321
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1755126
ClinVar RCV Id: RCV002375937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Thr41Asn
CA394301700
NM_021055.3:c.122C>A