Allele Registry

Canonical Allele Identifier: PA123642

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000014984

ClinVar Variation:

13956

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Pro198Thr	CA009290 NM_020975.6:c.592C>A