Canonical Allele Identifier: PA2580257015
Gene: C9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1906044
ClinVar RCV Id: RCV002583965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001728.1:p.His384Leu
CA117170980
NM_001737.5:c.1151A>T