Canonical Allele Identifier: PA2829972832
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49680
ClinVar RCV Id: RCV000042942 RCV000201010 RCV002468995
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Leu410Arg
CA014118
NM_021055.3:c.1229T>G