Allele Registry

Canonical Allele Identifier: PA2828047612

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000431229

ClinVar Variation:

24916

HGVS (amino-acid)	Matching Registered Transcripts
NP_001342145.1:p.Asp377Gly	CA008219 NM_001355216.1:c.1130A>G