Canonical Allele Identifier: PA2580117018
Gene: SLC35E4 HGNC NCBI
ClinVar RCV:
RCV004167998
ClinVar Variation:
2319096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001479.1:p.Thr279Ile
CA411212890
NM_001001479.4:c.836C>T