Allele Registry

Canonical Allele Identifier: PA645450569

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000472212

RCV000566718

RCV001107048

RCV001107049

RCV001107050

RCV001107714

ClinVar Variation:

405539

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Leu389Phe	CA16613014 NM_020975.6:c.1165C>T