Allele Registry

Canonical Allele Identifier: PA106613

Gene: RET HGNC NCBI

ClinVar RCV:

RCV003219010

ClinVar Variation:

2497944

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Cys609Trp	CA007855 NM_020975.6:c.1827C>G