Allele Registry

Canonical Allele Identifier: PA2499287517

Gene: RET HGNC NCBI

ClinVar Variation Id: 1002688

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Met868Ile	CA376556841 NM_020975.6:c.2604G>A CA376556842 NM_020975.6:c.2604G>C CA376556844 NM_020975.6:c.2604G>T