Canonical Allele Identifier: PA2825576599
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405956
ClinVar RCV Id: RCV000458532 RCV000500804 RCV001022474 RCV004000678
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ala1456Thr
CA16615031
NM_001114382.3:c.4366G>A