Allele Registry

Canonical Allele Identifier: PA2828047486

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000021784

RCV000412987

RCV000565237

RCV003062257

ClinVar Variation:

24898

2136858

HGVS (amino-acid)	Matching Registered Transcripts
NP_001342145.1:p.Cys357Tyr	CA007894 NM_001355216.1:c.1070_1071delinsAT CA007934 NM_001355216.1:c.1070G>A