Allele Registry

Canonical Allele Identifier: PA2829942140

Gene: RET HGNC NCBI

ClinVar Variation Id: 486338

HGVS (amino-acid)	Matching Registered Transcripts
NP_065681.1:p.Ser832Arg	CA039457 NM_020630.6:c.2496C>G CA376556382 NM_020630.6:c.2494A>C CA376556386 NM_020630.6:c.2496C>A