Canonical Allele Identifier: PA2828412890
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238000
ClinVar RCV Id: RCV000232107 RCV000413302 RCV002433957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Asn941Asp
CA10583315
NM_001370404.1:c.2821A>G