Canonical Allele Identifier: PA2829407980
Gene: NPM1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002511.1:p.Asp178His
CA362133941
NM_002520.7:c.532G>C