Canonical Allele Identifier: PA2827003108
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49241
ClinVar RCV Id: RCV000042500 RCV000201071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Arg952Pro
CA018497
NM_001318827.2:c.2855G>C