Allele Registry

Canonical Allele Identifier: PA2828049137

Gene: RET HGNC NCBI

ClinVar RCV:

RCV002591722

ClinVar Variation:

2179095

HGVS (amino-acid)	Matching Registered Transcripts
NP_001342145.1:p.Pro785Arg	CA376558427 NM_001355216.1:c.2354C>G