Canonical Allele Identifier: PA2827005110
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 424444
ClinVar RCV Id: RCV000480140 RCV000555170
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Val1543Met
CA16620103
NM_001318827.2:c.4627G>A