Canonical Allele Identifier: PA2827001558
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467887
ClinVar RCV Id: RCV000542715 RCV002395406 RCV003314613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Asp512Gly
CA394267934
NM_001318827.2:c.1535A>G