Allele Registry

Canonical Allele Identifier: PA2828047615

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000219970

RCV002513161

ClinVar Variation:

24914

HGVS (amino-acid)	Matching Registered Transcripts
NP_001342145.1:p.Asp377Tyr	CA008198 NM_001355216.1:c.1129G>T