Canonical Allele Identifier: PA2827002779
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1488823
ClinVar RCV Id: RCV001980328
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Asn845Lys
CA394279170
NM_001318827.2:c.2535T>A
CA394279172
NM_001318827.2:c.2535T>G