Canonical Allele Identifier: PA2828410359
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 516774
ClinVar RCV Id: RCV000729897 RCV001024992 RCV001087306 RCV002469218
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Val207Ile
CA055776
NM_001370404.1:c.619G>A