Allele Registry

Canonical Allele Identifier: PA2828046440

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000014952

ClinVar Variation:

13927

HGVS (amino-acid)	Matching Registered Transcripts
NP_001342145.1:p.Phe139Leu	CA007467 NM_001355216.1:c.417C>A CA376547659 NM_001355216.1:c.415T>C CA376547674 NM_001355216.1:c.417C>G