Allele Registry

Canonical Allele Identifier: PA2828323464

Gene: NAP1L4 HGNC NCBI

ClinVar RCV:

RCV004163970

ClinVar Variation:

2318573

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356305.1:p.Ile56Val	CA5823488 NM_001369376.1:c.166A>G