Canonical Allele Identifier: PA2828413990
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406066
ClinVar RCV Id: RCV000475183 RCV001021517 RCV001088738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Asp1275Asn
CA049735
NM_001370404.1:c.3823G>A