Allele Registry

Canonical Allele Identifier: PA658670413

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000538127

RCV002380630

RCV002384265

RCV003231531

RCV003444270

RCV004007298

RCV004527658

ClinVar Variation:

477312

1769192

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Ala432Val	CA032968 NM_020975.6:c.1295C>T CA206261326 NM_020975.6:c.1295_1296delinsTG