Allele Registry

Canonical Allele Identifier: PA2829949423

Gene: RET HGNC NCBI

ClinVar RCV:

RCV001360302

ClinVar Variation:

1052170

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Thr1038Ser	CA376558421 NM_020975.6:c.3112A>T