Canonical Allele Identifier: PA2825181180
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1372634
ClinVar RCV Id: RCV001874715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.His495Tyr
CA394325875
NM_000548.5:c.1483C>T