Allele Registry

Canonical Allele Identifier: PA106833

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000014922

RCV000014923

RCV000182581

RCV000654584

RCV001013616

RCV001310209

RCV001420921

ClinVar Variation:

13908

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Cys634Gly	CA008324 NM_020975.6:c.1900T>G