Allele Registry

Canonical Allele Identifier: PA350071

Gene: RET HGNC NCBI

ClinVar Variation Id: 220266

HGVS (amino-acid)	Matching Registered Transcripts
NP_065681.1:p.Met848Ile	CA039702 NM_020630.6:c.2544G>A CA376556524 NM_020630.6:c.2544G>C CA376556525 NM_020630.6:c.2544G>T