Allele Registry

Canonical Allele Identifier: PA2573171564

Gene: C7 HGNC NCBI

ClinVar RCV:

RCV001984446

RCV002479703

ClinVar Variation:

1493533

HGVS (amino-acid)	Matching Registered Transcripts
NP_000578.2:p.Gln415Arg	CA3249894 NM_000587.4:c.1244A>G