Allele Registry

Canonical Allele Identifier: PA105065

Gene: FAM20C HGNC NCBI

ClinVar RCV:

RCV000001080

RCV002512632

ClinVar Variation:

1025

HGVS (amino-acid)	Matching Registered Transcripts
NP_064608.2:p.Arg549Trp	CA250013 NM_020223.4:c.1645C>T