Canonical Allele Identifier: PA2829340203
Gene: C1S HGNC NCBI

Linked Data

ClinVar Variation Id: 1369281
ClinVar RCV Id: RCV001894862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001725.1:p.Ala11Leu
CA2573148408
NM_001734.5:c.31_32delinsTT