Allele Registry

Canonical Allele Identifier: PA2580316269

Gene: NAP1L4 HGNC NCBI

ClinVar RCV:

RCV004163970

ClinVar Variation:

2318573

HGVS (amino-acid)	Matching Registered Transcripts
NP_005960.1:p.Ile56Val	CA5823488 NM_005969.4:c.166A>G