Canonical Allele Identifier: PA2828417696
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_001357334.1:p.Lys574Arg
CA16614928
NM_001370405.1:c.1721A>G