Allele Registry

Canonical Allele Identifier: PA095128

Gene: C2 HGNC NCBI

ClinVar RCV:

RCV000012911

ClinVar Variation:

12128

HGVS (amino-acid)	Matching Registered Transcripts
NP_000054.2:p.Ser209Phe	CA136929237 NM_000063.6:c.626C>T