Allele Registry

Canonical Allele Identifier: PA106692

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000014919

RCV000228834

RCV000522833

RCV000762807

RCV002408462

RCV002470710

ClinVar Variation:

13905

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