Canonical Allele Identifier: PA2827009001
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1735113
ClinVar RCV Id: RCV002355213 RCV003102451
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Asn1178His
CA394293629
NM_001318829.2:c.3532A>C