Canonical Allele Identifier: PA2827001751
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207722
ClinVar RCV Id: RCV000189988 RCV001236049
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Lys562Arg
CA033543
NM_001318827.2:c.1685A>G