Canonical Allele Identifier: PA2825577337
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486644
ClinVar RCV Id: RCV000567505 RCV001065808 RCV001764691 RCV003465277
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Asn1658Asp
CA394311437
NM_001114382.3:c.4972A>G