Allele Registry

Canonical Allele Identifier: PA1139738613

Gene: RET HGNC NCBI

ClinVar RCV:

RCV001055064

RCV002249661

ClinVar Variation:

850811

HGVS (amino-acid)	Matching Registered Transcripts
NP_001342145.1:p.Arg59Leu	CA206257455 NM_001355216.1:c.176G>T