Allele Registry

Canonical Allele Identifier: PA215912

Gene: RET HGNC NCBI

Linked Data

ClinVar RCV:

RCV000034777

RCV000123327

RCV000148775

RCV000223157

RCV000573525

RCV000663296

RCV001103896

RCV001103897

RCV001103898

RCV001104177

RCV001269367

RCV004528165

ClinVar Variation:

41845

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_065681.1:p.Val262Ala	CA009350 NM_020630.6:c.785T>C