Allele Registry

Canonical Allele Identifier: PA197798

Gene: RET HGNC NCBI

ClinVar Allele:

182949

ClinVar RCV:

RCV000167232

RCV000553159

RCV002485039

ClinVar Variation:

187498

HGVS (amino-acid)	Matching Registered Transcripts
NP_065681.1:p.Val351Ile	CA007417 NM_020630.6:c.1051G>A