Allele Registry

Canonical Allele Identifier: PA128452

Gene: RET HGNC NCBI

ClinVar RCV:

RCV000757722

RCV001267835

ClinVar Variation:

24963

HGVS (amino-acid)	Matching Registered Transcripts
NP_066124.1:p.Ser904Phe	CA009027 NM_020975.6:c.2711C>T