Canonical Allele Identifier: PA2829980742
Gene: XYLT2 HGNC NCBI
ClinVar RCV:
RCV004485771
ClinVar Variation:
3191381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071450.2:p.Val92Met
CA8646122
NM_022167.4:c.274G>A