Canonical Allele Identifier: PA2825922123
Gene: C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12128
ClinVar RCV Id: RCV000012911

Amino-acid Alleles

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