Canonical Allele Identifier: PA2827001483
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64901
ClinVar RCV Id: RCV000055102 RCV003441735 RCV003512005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Leu491Pro
CA015160
NM_001318827.2:c.1472T>C