Allele Registry

Canonical Allele Identifier: PA106670

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000021784

RCV000412987

RCV000565237

RCV003062257

ClinVar Variation:

24898

2136858

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Cys611Tyr	CA007894 NM_020975.6:c.1832_1833delinsAT CA007934 NM_020975.6:c.1832G>A