Allele Registry

Canonical Allele Identifier: PA2573275527

Gene: FAM20C HGNC NCBI

ClinVar RCV:

RCV001939133

RCV002560650

ClinVar Variation:

1429840

HGVS (amino-acid)	Matching Registered Transcripts
NP_064608.2:p.Gly266Trp	CA152235913 NM_020223.4:c.796G>T