Allele Registry

Canonical Allele Identifier: PA128326

Gene: RET HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

36273

233786

ClinVar RCV:

RCV000082052

RCV000174156

RCV000219014

RCV000467461

RCV000556223

RCV000570730

RCV001027731

RCV001535750

RCV001589145

RCV001818173

RCV002265692

RCV002463360

RCV002477001

RCV003137821

RCV003335051

RCV003458339

RCV003460489

RCV003462451

RCV004532784

ClinVar Variation:

24932

230926

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Lys666Asn	CA008525 NM_020975.6:c.1998G>T CA036775 NM_020975.6:c.1998G>C