Canonical Allele Identifier: PA2573171584
Gene: C7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1384929
ClinVar RCV Id: RCV001902704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000578.2:p.Ile606Val
CA3250098
NM_000587.4:c.1816A>G