Allele Registry

Canonical Allele Identifier: PA2828046648

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000797130

RCV002386403

ClinVar Variation:

643435

HGVS (amino-acid)	Matching Registered Transcripts
NP_001342145.1:p.Ala178Glu	CA032939 NM_001355216.1:c.533C>A CA915945897 NM_001355216.1:c.533_534delinsAG