Canonical Allele Identifier: PA2827001639
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405989
ClinVar RCV Id: RCV000473481 RCV000561401 RCV003332174
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Lys537Arg
CA16614928
NM_001318827.2:c.1610A>G