Canonical Allele Identifier: PA645376693
Gene: FCRL6 HGNC NCBI

Linked Data

ClinVar Variation Id: 402860
ClinVar RCV Id: RCV000454785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001004310.2:p.Ser293Pro
CA1189792
NM_001004310.3:c.877T>C