Canonical Allele Identifier: PA2573095197
Gene: XYLT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1307685
ClinVar RCV Id: RCV001772540 RCV002034470 RCV004040164
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071449.1:p.Met545Val
CA7927830
NM_022166.4:c.1633A>G