Canonical Allele Identifier: PA2827001546
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406036
ClinVar RCV Id: RCV000477560 RCV002255385 RCV004000705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Pro506Ser
CA16615046
NM_001318827.2:c.1516C>T