Allele Registry

Canonical Allele Identifier: PA356919

Gene: RET HGNC NCBI

ClinVar Allele:

221957

ClinVar RCV:

RCV000206643

RCV000561732

RCV002285278

RCV002494521

ClinVar Variation:

219872

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Arg418Gln	CA032301 NM_020975.6:c.1253G>A