Canonical Allele Identifier: PA2825439527
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1427563
ClinVar RCV Id: RCV001945952
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Tyr1669Ser
CA054421
NM_001077183.3:c.5006A>C