Canonical Allele Identifier: PA2828410868
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49140
ClinVar RCV Id: RCV000042395 RCV000413741 RCV001065226
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Leu362Pro
CA013704
NM_001370404.1:c.1085T>C