Canonical Allele Identifier: PA2580451226
Gene: XYLT2 HGNC NCBI
ClinVar RCV:
RCV002919461
ClinVar Variation:
2316122
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071450.2:p.Arg424Cys
CA8646408
NM_022167.4:c.1270C>T