Canonical Allele Identifier: PA2827004696
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 536044
ClinVar RCV Id: RCV000644320 RCV002334136 RCV004004037
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Arg1426Trp
CA276754888
NM_001318827.2:c.4276C>T