Canonical Allele Identifier: PA2828393465
Gene: RFXANK HGNC NCBI

Linked Data

ClinVar Variation Id: 538593
ClinVar RCV Id: RCV000647950
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357166.1:p.Ala32Val
CA9322594
NM_001370237.1:c.95C>T