Canonical Allele Identifier: PA2499283863
Gene: NHP2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

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