Allele Registry

Canonical Allele Identifier: PA198347

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000167451

RCV000409277

RCV000409934

RCV000654567

RCV000764899

ClinVar Variation:

187701

HGVS (amino-acid)	Matching Registered Transcripts
NP_065681.1:p.Thr742Met	CA008602 NM_020630.6:c.2225C>T