Allele Registry

Canonical Allele Identifier: PA2826647692

Gene: C2 HGNC NCBI

ClinVar RCV:

RCV000012911

ClinVar Variation:

12128

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269388.1:p.Ser209Phe	CA136929237 NM_001282459.2:c.626C>T