Allele Registry

Canonical Allele Identifier: PA106513

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000014946

ClinVar Variation:

13921

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Arg897Gln	CA009008 NM_020975.6:c.2690G>A