Canonical Allele Identifier: PA2580257013
Gene: C9 HGNC NCBI
ClinVar RCV:
RCV003054487
ClinVar Variation:
2119091
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001728.1:p.Lys375Gln
CA359554850
NM_001737.5:c.1123A>C