Canonical Allele Identifier: PA2827005501
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_001305756.1:p.Arg1640Gly
CA022207
NM_001318827.2:c.4918C>G