Allele Registry

Canonical Allele Identifier: PA128385

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000478761

RCV000529442

RCV000567481

RCV000662806

ClinVar Variation:

24945

HGVS (amino-acid)	Matching Registered Transcripts
NP_065681.1:p.Arg833Cys	CA008813 NM_020630.6:c.2497C>T