Allele Registry

Canonical Allele Identifier: PA2829941972

Gene: RET HGNC NCBI

ClinVar RCV:

RCV002045273

ClinVar Variation:

1502831

HGVS (amino-acid)	Matching Registered Transcripts
NP_065681.1:p.Val778Phe	CA376555707 NM_020630.6:c.2332G>T