Allele Registry

Canonical Allele Identifier: PA2826647470

Gene: C2 HGNC NCBI

ClinVar RCV:

RCV000012911

ClinVar Variation:

12128

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269387.1:p.Ser180Phe	CA136929237 NM_001282458.2:c.539C>T