Allele Registry

Canonical Allele Identifier: PA2829941637

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000229577

RCV000662388

RCV001292757

RCV002411060

RCV002487084

RCV002508206

RCV003463677

ClinVar Variation:

241342

HGVS (amino-acid)	Matching Registered Transcripts
NP_065681.1:p.Ala641Thr	CA036607 NM_020630.6:c.1921G>A