Canonical Allele Identifier: PA339223
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 216726
ClinVar RCV Id: RCV000200291 RCV000283887 RCV000322527 RCV000374792 RCV000380664 RCV000572326 RCV000663300 RCV002470810
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Arg112Cys
CA043169
NM_020630.6:c.334C>T