Canonical Allele Identifier: PA658811195
Gene: RFXANK HGNC NCBI

Linked Data

ClinVar Variation Id: 538596

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003712.1:p.Asp149Asn
CA9322769
NM_003721.4:c.445G>A