Allele Registry

Canonical Allele Identifier: PA107075

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000014952

ClinVar Variation:

13927

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Phe393Leu	CA007467 NM_020975.6:c.1179C>A CA376547659 NM_020975.6:c.1177T>C CA376547674 NM_020975.6:c.1179C>G