Canonical Allele Identifier: PA2828393527
Gene: RFXANK HGNC NCBI

Linked Data

ClinVar Variation Id: 538596
ClinVar RCV Id: RCV000647953 RCV003945639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357166.1:p.Asp148Asn
CA9322769
NM_001370237.1:c.442G>A