Allele Registry

Canonical Allele Identifier: PA645450828

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000438390

RCV001228445

ClinVar Variation:

376313

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Glu632_Leu633del	CA008264 NM_020975.6:c.1896_1897delinsCG CA16602759 NM_020975.6:c.1894_1899del CA206262837 NM_020975.6:c.1895_1897del