Canonical Allele Identifier: PA2827004733
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405997
ClinVar RCV Id: RCV000470575 RCV002311771 RCV003463865
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Pro1435Ser
CA16615034
NM_001318827.2:c.4303C>T