Allele Registry

Canonical Allele Identifier: PA105100

Gene: FAM20C HGNC NCBI

ClinVar RCV:

RCV000001079

ClinVar Variation:

1024

HGVS (amino-acid)	Matching Registered Transcripts
NP_064608.2:p.Leu388Arg	CA250012 NM_020223.4:c.1163T>G