Canonical Allele Identifier: PA2825283004
Gene: CR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 939357
ClinVar RCV Id: RCV001208745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001006659.1:p.Pro560Thr
CA344533922
NM_001006658.3:c.1678C>A