Canonical Allele Identifier: PA2825181129
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1772993
ClinVar RCV Id: RCV002394649
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ile485Val
CA394325496
NM_000548.5:c.1453A>G