Canonical Allele Identifier: PA915970484
Gene: CLU HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001822.3:p.Asp328Asn
CA4690802
NM_001831.3:c.982G>A