Allele Registry

Canonical Allele Identifier: PA257032

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000014946

ClinVar Variation:

13921

HGVS (amino-acid)	Matching Registered Transcripts
NP_065681.1:p.Arg897Gln	CA009008 NM_020630.6:c.2690G>A