Canonical Allele Identifier: PA2829340237
Gene: C1S HGNC NCBI

Linked Data

ClinVar Variation Id: 1999070
ClinVar RCV Id: RCV002815136
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001725.1:p.Ser87Asn
CA383689010
NM_001734.5:c.260G>A