Canonical Allele Identifier: PA2741967443
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_060647.2:p.Pro1222Ala
CA356725154
NM_018177.6:c.3664C>G