Canonical Allele Identifier: PA2828414700
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_001357333.1:p.Ile1474Val
CA051585
NM_001370404.1:c.4420A>G