Allele Registry

Canonical Allele Identifier: PA106632

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000021782

RCV000736275

RCV004018655

ClinVar Variation:

24896

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Cys611Arg	CA007873 NM_020975.6:c.1831T>C