Canonical Allele Identifier: PA2827011569
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486602
ClinVar RCV Id: RCV000562822 RCV001049308 RCV004001145
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Thr878Ile
CA394279934
NM_001318829.2:c.2633C>T