Allele Registry

Canonical Allele Identifier: PA2825009156

Gene: C8B HGNC NCBI

ClinVar RCV:

RCV001521525

RCV003346601

ClinVar Variation:

1169777

HGVS (amino-acid)	Matching Registered Transcripts
NP_000057.3:p.Gly117Arg	CA876022 NM_000066.4:c.349G>A CA340510555 NM_000066.4:c.349G>C