Allele Registry

Canonical Allele Identifier: PA250060

Gene: FAM20C HGNC NCBI

ClinVar RCV:

RCV000023862

RCV002513209

ClinVar Variation:

30877

HGVS (amino-acid)	Matching Registered Transcripts
NP_064608.2:p.Gly266Arg	CA250059 NM_020223.4:c.796G>A CA366519456 NM_020223.4:c.796G>C