Canonical Allele Identifier: PA2827000260
Gene: TSC2 HGNC NCBI
ClinVar RCV:
RCV000644114
ClinVar Variation:
535892
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Thr110Lys
CA394308347
NM_001318827.2:c.329C>A