Canonical Allele Identifier: PA2828411398
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405944
ClinVar RCV Id: RCV000471506 RCV001012244 RCV001564370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ser526Asn
CA031083
NM_001370404.1:c.1577G>A