Canonical Allele Identifier: PA2829941832
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 580338
ClinVar RCV Id: RCV000703840 RCV000709118 RCV000708756 RCV001104665 RCV001104666 RCV001104667 RCV001104668 RCV002499266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Lys710Arg
CA037409
NM_020630.6:c.2129A>G