Allele Registry

Canonical Allele Identifier: PA161927

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000121984

RCV000793359

RCV002321602

ClinVar Variation:

135182

HGVS (amino-acid)	Matching Registered Transcripts
NP_065681.1:p.Pro1039Gln	CA009192 NM_020630.6:c.3116C>A