Canonical Allele Identifier: PA2829978358
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 954021
ClinVar RCV Id: RCV001226403
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Thr1032Asn
CA394285972
NM_021055.3:c.3095C>A