Canonical Allele Identifier: PA2828421668
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49834
ClinVar RCV Id: RCV000043100 RCV001249601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Arg1696Gly
CA022207
NM_001370405.1:c.5086C>G