Allele Registry

Canonical Allele Identifier: PA250062

Gene: FAM20C HGNC NCBI

ClinVar RCV:

RCV000023863

ClinVar Variation:

30878

HGVS (amino-acid)	Matching Registered Transcripts
NP_064608.2:p.Pro328Ser	CA250061 NM_020223.4:c.982C>T