Allele Registry

Canonical Allele Identifier: PA259289

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000219970

RCV002513161

ClinVar Variation:

24914

HGVS (amino-acid)	Matching Registered Transcripts
NP_065681.1:p.Asp631Tyr	CA008198 NM_020630.6:c.1891G>T