Canonical Allele Identifier: PA2826614289
Gene: RFXANK HGNC NCBI

Linked Data

ClinVar Variation Id: 328648
ClinVar RCV Id: RCV000525677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265656.1:p.Gln229Glu
CA9322949
NM_001278727.2:c.685C>G