Canonical Allele Identifier: PA2827011023
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 651314
ClinVar RCV Id: RCV000806641 RCV003461161 RCV003380734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Thr1618Ala
CA394314229
NM_001318829.2:c.4852A>G