Canonical Allele Identifier: PA2828417459
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 836730
ClinVar RCV Id: RCV001037922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.His502Asn
CA394326069
NM_001370405.1:c.1504C>A