Canonical Allele Identifier: PA2829979441
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49528
ClinVar RCV Id: RCV000042788 RCV000996158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Trp1165Arg
CA019404
NM_021055.3:c.3493T>C
CA394291505
NM_021055.3:c.3493T>A