Allele Registry

Canonical Allele Identifier: PA2829949430

Gene: RET HGNC NCBI

ClinVar RCV:

RCV002591722

ClinVar Variation:

2179095

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Pro1039Arg	CA376558427 NM_020975.6:c.3116C>G