Allele Registry

Canonical Allele Identifier: PA106803

Gene: RET HGNC NCBI

ClinVar RCV:

RCV002407971

ClinVar Variation:

1782016

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Cys630Ser	CA008164 NM_020975.6:c.1889G>C CA376552896 NM_020975.6:c.1888T>A