Canonical Allele Identifier: PA2829977224
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1488823
ClinVar RCV Id: RCV001980328

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Asn882Lys
CA394279170
NM_021055.3:c.2646T>A
CA394279172
NM_021055.3:c.2646T>G