Canonical Allele Identifier: PA2827000070
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1379252
ClinVar RCV Id: RCV001914808 RCV003303276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Thr41Ala
CA394301694
NM_001318827.2:c.121A>G