Canonical Allele Identifier: PA106692
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13905
ClinVar RCV Id: RCV000014919 RCV000228834 RCV000522833 RCV000762807 RCV002408462 RCV002470710
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Cys618Gly
CA007995
NM_020975.6:c.1852T>G