Canonical Allele Identifier: PA2827017718
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2706252
ClinVar RCV Id: RCV003512940
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ala519Pro
CA394326234
NM_001318832.2:c.1555G>C