Canonical Allele Identifier: PA2826988093
Gene: N4BP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2612757
ClinVar RCV Id: RCV004354386
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305288.1:p.Pro1142Ala
CA356725154
NM_001318359.2:c.3424C>G