Canonical Allele Identifier: PA2826989509
Gene: SLC35E4 HGNC NCBI
ClinVar RCV:
RCV004459290
ClinVar Variation:
3164402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305299.1:p.Val18Ala
CA10185096
NM_001318370.1:c.53T>C