Allele Registry

Canonical Allele Identifier: PA2499233721

Gene: C7 HGNC NCBI

ClinVar RCV:

RCV001520303

RCV001529247

ClinVar Variation:

1169276

HGVS (amino-acid)	Matching Registered Transcripts
NP_000578.2:p.Thr587Pro	CA3250085 NM_000587.4:c.1759A>C