Canonical Allele Identifier: PA1139676483
Gene: CR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 993828
ClinVar RCV Id: RCV001812917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000642.3:p.Val2125Leu
CA1370428
NM_000651.6:c.6373G>T
CA1370429
NM_000651.6:c.6373G>C