Canonical Allele Identifier: PA2825185745
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1733615
ClinVar RCV Id: RCV002452497
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Pro1218His
CA394291998
NM_000548.5:c.3653C>A