Canonical Allele Identifier: PA2829983438
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 449584
ClinVar RCV Id: RCV000519477 RCV002527581 RCV003159666
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Asn1688Asp
CA394314156
NM_021055.3:c.5062A>G