Allele Registry

Canonical Allele Identifier: PA2829941777

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000705637

RCV002422601

ClinVar Variation:

581727

HGVS (amino-acid)	Matching Registered Transcripts
NP_065681.1:p.Gly691Arg	CA376553251 NM_020630.6:c.2071G>C