Canonical Allele Identifier: PA2829939317
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 477345
ClinVar RCV Id: RCV000528844 RCV001015313 RCV002483498
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Arg79Gln
CA376770372
NM_020630.6:c.236G>A