Canonical Allele Identifier: PA2828421529
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207693
ClinVar RCV Id: RCV000462184 RCV002336505 RCV001721233 RCV003996873 RCV004539758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Asn1664Ser
CA054000
NM_001370405.1:c.4991A>G