Canonical Allele Identifier: PA2580415541
Gene: NHP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2071769
ClinVar RCV Id: RCV002962395
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060308.1:p.Pro131Thr
CA3589112
NM_017838.4:c.391C>A