Allele Registry

Canonical Allele Identifier: PA106702

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000255102

RCV000548660

RCV000571381

RCV004018656

ClinVar Variation:

24902

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Cys618Phe	CA008022 NM_020975.6:c.1853G>T