Canonical Allele Identifier: PA2828411962
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535899
ClinVar RCV Id: RCV000644122 RCV001014079 RCV002499096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Gly671Asp
CA035599
NM_001370404.1:c.2012G>A