Allele Registry

Canonical Allele Identifier: PA117345

Gene: FRZB HGNC NCBI

ClinVar Allele:

20260

ClinVar RCV:

RCV000005531

RCV003964795

ClinVar Variation:

5221

HGVS (amino-acid)	Matching Registered Transcripts
NP_001454.2:p.Arg200Trp	CA117344 NM_001463.4:c.598C>T