Allele Registry

Canonical Allele Identifier: PA257038

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000014948

RCV000678742

RCV002514098

ClinVar Variation:

13923

HGVS (amino-acid)	Matching Registered Transcripts
NP_065681.1:p.Ser32Leu	CA009398 NM_020630.6:c.95C>T