Canonical Allele Identifier: PA2826614371
Gene: RFXANK HGNC NCBI

Linked Data

ClinVar Variation Id: 538596
ClinVar RCV Id: RCV000647953 RCV003945639
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265657.1:p.Asp126Asn
CA9322769
NM_001278728.2:c.376G>A