Allele Registry

Canonical Allele Identifier: PA2828048885

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000014947

ClinVar Variation:

13922

HGVS (amino-acid)	Matching Registered Transcripts
NP_001342145.1:p.Arg718Gly	CA009130 NM_001355216.1:c.2152A>G