Allele Registry

Canonical Allele Identifier: PA1139741468

Gene: RET HGNC NCBI

ClinVar RCV:

RCV001231313

ClinVar Variation:

958196

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Cys630Gly	CA376552897 NM_020975.6:c.1888T>G