Allele Registry

Canonical Allele Identifier: PA106644

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000506649

ClinVar Variation:

24897

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Cys611Gly	CA007883 NM_020975.6:c.1831T>G