Canonical Allele Identifier: PA2829972792
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467848
ClinVar RCV Id: RCV000545351 RCV001010318 RCV003999246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Gly402Arg
CA028779
NM_021055.3:c.1204G>A
CA394320813
NM_021055.3:c.1204G>C