Canonical Allele Identifier: PA2828417859
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12397
ClinVar RCV Id: RCV000013205 RCV000055317 RCV000042946 RCV000414340 RCV000491426 RCV000768118
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Arg611Gln
CA015920
NM_001370405.1:c.1832G>A