Allele Registry

Canonical Allele Identifier: PA2580440663

Gene: FAM20C HGNC NCBI

ClinVar RCV:

RCV002901056

ClinVar Variation:

2308744

HGVS (amino-acid)	Matching Registered Transcripts
NP_064608.2:p.Ile246Thr	CA152226803 NM_020223.4:c.737T>C