Canonical Allele Identifier: PA2499248203
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1010404
ClinVar RCV Id: RCV001308024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Thr988Asn
CA394285777
NM_001318827.2:c.2963C>A