Allele Registry

Canonical Allele Identifier: PA2829941779

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000699283

RCV003372819

ClinVar Variation:

576718

HGVS (amino-acid)	Matching Registered Transcripts
NP_065681.1:p.Gly691Cys	CA376553252 NM_020630.6:c.2071G>T