Allele Registry

Canonical Allele Identifier: PA130242

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000570795

RCV000709106

RCV001046577

RCV001262456

ClinVar Variation:

38594

HGVS (amino-acid)	Matching Registered Transcripts
NP_065681.1:p.Thr338Ile	CA007399 NM_020630.6:c.1013C>T