Canonical Allele Identifier: PA2828393438
Gene: RFXANK HGNC NCBI

Linked Data

ClinVar Variation Id: 328648
ClinVar RCV Id: RCV000525677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357165.1:p.Gln250Glu
CA9322949
NM_001370236.1:c.748C>G