Canonical Allele Identifier: PA2580444349
Gene: XK HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066569.1:p.Leu24Gln
CA10383507
NM_021083.4:c.71T>A