Allele Registry

Canonical Allele Identifier: PA106602

Gene: RET HGNC NCBI

ClinVar RCV:

RCV004589374

RCV004950822

ClinVar Variation:

3254419

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Cys609Gly	CA007815 NM_020975.6:c.1825T>G