Allele Registry

Canonical Allele Identifier: PA2828048383

Gene: RET HGNC NCBI

ClinVar Variation Id: 1481838

HGVS (amino-acid)	Matching Registered Transcripts
NP_001342145.1:p.Ser565Arg	CA376556228 NM_001355216.1:c.1693A>C CA376556240 NM_001355216.1:c.1695C>A CA376556242 NM_001355216.1:c.1695C>G