Allele Registry

Canonical Allele Identifier: PA338675

Gene: RET HGNC NCBI

ClinVar Allele:

212772

ClinVar RCV:

RCV000199477

RCV000574518

RCV000662571

RCV002284372

RCV002485323

RCV003462340

ClinVar Variation:

216731

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Gln326Arg	CA338671 NM_020975.6:c.977A>G