Canonical Allele Identifier: PA2827009726
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468098
ClinVar RCV Id: RCV000548577 RCV000571084 RCV001546708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ile1403Val
CA051585
NM_001318829.2:c.4207A>G