Allele Registry

Canonical Allele Identifier: PA2825645494

Gene: FCGR3A HGNC NCBI

ClinVar RCV:

RCV000455498

ClinVar Variation:

225994

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121067.1:p.Phe176Val	CA1211378 NM_001127595.2:c.526T>G