Canonical Allele Identifier: PA2828420413
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207682
ClinVar RCV Id: RCV000189928 RCV001852522 RCV003298247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Asp1357Asn
CA319383
NM_001370405.1:c.4069G>A