Allele Registry

Canonical Allele Identifier: PA106289

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000797130

RCV002386403

ClinVar Variation:

643435

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Ala432Glu	CA032939 NM_020975.6:c.1295C>A CA915945897 NM_020975.6:c.1295_1296delinsAG