Canonical Allele Identifier: PA339224
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 216726
ClinVar RCV Id: RCV000200291 RCV000283887 RCV000322527 RCV000374792 RCV000380664 RCV000572326 RCV000663300 RCV002470810
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Arg112Cys
CA043169
NM_020975.6:c.334C>T