Allele Registry

Canonical Allele Identifier: PA2828047593

Gene: RET HGNC NCBI

ClinVar RCV:

RCV002407971

ClinVar Variation:

1782016

HGVS (amino-acid)	Matching Registered Transcripts
NP_001342145.1:p.Cys376Ser	CA008164 NM_001355216.1:c.1127G>C CA376552896 NM_001355216.1:c.1126T>A