Allele Registry

Canonical Allele Identifier: PA2828323614

Gene: NAP1L4 HGNC NCBI

ClinVar Allele:

2310934

ClinVar RCV:

RCV004163970

ClinVar Variation:

2318573

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356311.1:p.Ile56Val	CA5823488 NM_001369382.1:c.166A>G