Canonical Allele Identifier: PA2827001484
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2752998
ClinVar RCV Id: RCV003511782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Leu491Val
CA394326701
NM_001318827.2:c.1471C>G