Allele Registry

Canonical Allele Identifier: PA2826606460

Gene: C8B HGNC NCBI

ClinVar RCV:

RCV001521525

RCV003346601

ClinVar Variation:

1169777

HGVS (amino-acid)	Matching Registered Transcripts
NP_001265473.2:p.Gly55Arg	CA876022 NM_001278544.2:c.163G>A CA340510555 NM_001278544.2:c.163G>C