Canonical Allele Identifier: PA2827000898
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64956
ClinVar RCV Id: RCV000055159 RCV001009773 RCV001079443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Lys310Arg
CA013642
NM_001318827.2:c.929A>G