Canonical Allele Identifier: PA2827008593
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535973
ClinVar RCV Id: RCV000644221 RCV001565707 RCV004004016
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Arg1037His
CA394286758
NM_001318829.2:c.3110G>A