Canonical Allele Identifier: PA2826988094
Gene: N4BP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2354211
ClinVar RCV Id: RCV004190532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305288.1:p.Ala1145Ser
CA356725190
NM_001318359.2:c.3433G>T