Canonical Allele Identifier: PA2829341006
Gene: C5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1444040

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001726.2:p.Ile1671Val
CA5216995
NM_001735.3:c.5011A>G