Canonical Allele Identifier: PA645406504
Gene: C3 HGNC NCBI

Linked Data

ClinVar Variation Id: 330302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000055.2:p.Ile900Met
CA9128993
NM_000064.4:c.2700C>G