Allele Registry

Canonical Allele Identifier: PA106399

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000014957

RCV000566081

RCV000654592

RCV000662693

RCV002476968

RCV003114192

ClinVar Variation:

13932

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Arg313Gln	CA009384 NM_020975.6:c.938G>A