Allele Registry

Canonical Allele Identifier: PA916043135

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000121983

RCV000409698

RCV000412388

RCV000532140

RCV001577914

RCV002321601

RCV003460860

ClinVar Variation:

135181

HGVS (amino-acid)	Matching Registered Transcripts
NP_001342145.1:p.Tyr808Cys	CA009211 NM_001355216.1:c.2423A>G