Allele Registry

Canonical Allele Identifier: PA161924

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000121983

RCV000409698

RCV000412388

RCV000532140

RCV001577914

RCV002321601

RCV003460860

ClinVar Variation:

135181

HGVS (amino-acid)	Matching Registered Transcripts
NP_065681.1:p.Tyr1062Cys	CA009211 NM_020630.6:c.3185A>G