Canonical Allele Identifier: PA915968942
Gene: C9 HGNC NCBI
ClinVar RCV:
RCV000998375
ClinVar Variation:
809750
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001728.1:p.Asp454Asn
CA3246722
NM_001737.5:c.1360G>A