Allele Registry

Canonical Allele Identifier: PA127063

Gene: C3 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

32095

2932843

ClinVar RCV:

RCV000018584

RCV000018585

RCV000395565

RCV001521403

RCV002293984

RCV002444434

RCV003578778

ClinVar Variation:

17056

2769528

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000055.2:p.Arg102Gly	CA127061 NM_000064.4:c.304C>G CA2697556137 NM_000064.4:c.303_304delinsAG