Allele Registry

Canonical Allele Identifier: PA2573275574

Gene: FAM20C HGNC NCBI

ClinVar Variation Id: 1369846

HGVS (amino-acid)	Matching Registered Transcripts
NP_064608.2:p.Arg551Cys	CA4109211 NM_020223.4:c.1651C>T