Allele Registry

Canonical Allele Identifier: PA2829940708

Gene: RET HGNC NCBI

ClinVar RCV:

RCV001980489

ClinVar Variation:

1489156

HGVS (amino-acid)	Matching Registered Transcripts
NP_065681.1:p.Ala432Gly	CA376548925 NM_020630.6:c.1295C>G CA2573145051 NM_020630.6:c.1295_1296delinsGG