Allele Registry

Canonical Allele Identifier: PA645450498

Gene: RET HGNC NCBI

ClinVar Allele:

397445

ClinVar RCV:

RCV000470242

RCV001025355

RCV001570499

RCV002502615

RCV004529585

ClinVar Variation:

405525

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Ala217Asp	CA16612872 NM_020975.6:c.650C>A