Allele Registry

Canonical Allele Identifier: PA106380

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000014964

ClinVar Variation:

13937

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Arg231His	CA009319 NM_020975.6:c.692G>A