Allele Registry

Canonical Allele Identifier: PA128248

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000431229

ClinVar Variation:

24916

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Asp631Gly	CA008219 NM_020975.6:c.1892A>G