Canonical Allele Identifier: PA2827004621
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 187598
ClinVar RCV Id: RCV000167342 RCV001230620 RCV001753574
ClinVar Variation Id: 468097
ClinVar RCV Id: RCV000535938 RCV000568343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Phe1406Leu
CA020614
NM_001318827.2:c.4218C>A
CA394302825
NM_001318827.2:c.4216T>C
CA394302842
NM_001318827.2:c.4218C>G