Canonical Allele Identifier: PA2827008192
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12403
ClinVar RCV Id: RCV000013212 RCV000042875 RCV000221069 RCV000255572 RCV002482858 RCV004532330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Arg856Gln
CA017951
NM_001318829.2:c.2567G>A