Canonical Allele Identifier: PA128216
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13916
ClinVar RCV Id: RCV000014936 RCV000021801 RCV000413879 RCV000420281 RCV000428368 RCV000431330 RCV000441133 RCV000678747 RCV002408464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Cys620Tyr
CA008076
NM_020630.6:c.1859G>A