Canonical Allele Identifier: PA2828392953
Gene: RFXANK HGNC NCBI

Linked Data

ClinVar Variation Id: 328648
ClinVar RCV Id: RCV000525677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357162.1:p.Gln251Glu
CA9322949
NM_001370233.1:c.751C>G