Allele Registry

Canonical Allele Identifier: PA2573185316

Gene: C2 HGNC NCBI

ClinVar RCV:

RCV000012911

ClinVar Variation:

12128

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171534.1:p.Ser86Phe	CA136929237 NM_001178063.3:c.257C>T