Allele Registry

Canonical Allele Identifier: PA2829941708

Gene: RET HGNC NCBI

ClinVar RCV:

RCV001349419

RCV002420753

ClinVar Variation:

1045072

HGVS (amino-acid)	Matching Registered Transcripts
NP_065681.1:p.Lys666Gln	CA036741 NM_020630.6:c.1996A>C