Canonical Allele Identifier: PA2826614316
Gene: RFXANK HGNC NCBI

Linked Data

ClinVar Variation Id: 538593
ClinVar RCV Id: RCV000647950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265657.1:p.Ala32Val
CA9322594
NM_001278728.2:c.95C>T