Canonical Allele Identifier: PA2826647334
Gene: C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 356249
ClinVar RCV Id: RCV000285510 RCV000329987 RCV000379644 RCV001095044 RCV002058586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269386.1:p.Ala226Thr
CA3727699
NM_001282457.2:c.676G>A