Canonical Allele Identifier: PA123628
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13933
ClinVar RCV Id: RCV000014958 RCV000168107 RCV000082049 RCV000173889 RCV000441078 RCV000444552 RCV000496009 RCV000509116 RCV000424503 RCV000431942 RCV000562113 RCV003460480 RCV004532352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Cys609Tyr
CA007824
NM_020630.6:c.1826G>A