Canonical Allele Identifier: PA2828323689
Gene: NAP1L4 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356314.1:p.Ile56Val
CA5823488
NM_001369385.1:c.166A>G