Allele Registry

Canonical Allele Identifier: PA2825922123

Gene: C2 HGNC NCBI

ClinVar RCV:

RCV000012911

ClinVar Variation:

12128

HGVS (amino-acid)	Matching Registered Transcripts
NP_001139375.1:p.Ser77Phe	CA136929237 NM_001145903.3:c.230C>T