Canonical Allele Identifier: PA2828410996
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_001357333.1:p.Gly402Arg
CA028779
NM_001370404.1:c.1204G>A
CA394320813
NM_001370404.1:c.1204G>C