Allele Registry

Canonical Allele Identifier: PA106661

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000014932

RCV002513055

ClinVar Variation:

13913

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Cys611Trp	CA007954 NM_020975.6:c.1833C>G