Canonical Allele Identifier: PA2828421559
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49931
ClinVar RCV Id: RCV000043198 RCV000201077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Arg1670Pro
CA021846
NM_001370405.1:c.5009G>C