Allele Registry

Canonical Allele Identifier: PA250058

Gene: FAM20C HGNC NCBI

ClinVar RCV:

RCV000023861

ClinVar Variation:

30876

HGVS (amino-acid)	Matching Registered Transcripts
NP_064608.2:p.Ile246Asn	CA250057 NM_020223.4:c.737T>A