Canonical Allele Identifier: PA645406620
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 330271
ClinVar RCV Id: RCV000279318 RCV000337839 RCV000395497 RCV001281035 RCV000948468 RCV001820990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Ser1619Arg
CA9128209
NM_000064.4:c.4855A>C
CA403610764
NM_000064.4:c.4857C>G
CA403610765
NM_000064.4:c.4857C>A