Allele Registry

Canonical Allele Identifier: PA2829939436

Gene: RET HGNC NCBI

ClinVar Variation Id: 1729813

HGVS (amino-acid)	Matching Registered Transcripts
NP_065681.1:p.Ser110Arg	CA376770583 NM_020630.6:c.328A>C CA376770588 NM_020630.6:c.330T>A CA376770589 NM_020630.6:c.330T>G