Allele Registry

Canonical Allele Identifier: PA2829941837

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000465229

RCV003470404

ClinVar Variation:

405531

HGVS (amino-acid)	Matching Registered Transcripts
NP_065681.1:p.Leu712Pro	CA037424 NM_020630.6:c.2135T>C