Allele Registry

Canonical Allele Identifier: PA2580522558

Gene: FAM81A HGNC NCBI

ClinVar RCV:

RCV004185644

ClinVar Variation:

2341719

HGVS (amino-acid)	Matching Registered Transcripts
NP_689663.2:p.Phe291Ser	CA7590784 NM_152450.3:c.872T>C