Canonical Allele Identifier: PA2573221031
Gene: C9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1416140
ClinVar RCV Id: RCV001935548
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001728.1:p.Arg369Trp
CA3246805
NM_001737.5:c.1105C>T