Allele Registry

Canonical Allele Identifier: PA2828047625

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000438390

RCV001228445

ClinVar Variation:

376313

HGVS (amino-acid)	Matching Registered Transcripts
NP_001342145.1:p.Glu378_Leu379del	CA008264 NM_001355216.1:c.1134_1135delinsCG CA16602759 NM_001355216.1:c.1132_1137del CA206262837 NM_001355216.1:c.1133_1135del