Canonical Allele Identifier: PA2499283863
Gene: NHP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1026003
ClinVar RCV Id: RCV001326399
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060308.1:p.Asp140Asn
CA362391007
NM_017838.4:c.418G>A