Canonical Allele Identifier: PA2830369260
Gene: DPY19L2 HGNC NCBI
ClinVar RCV:
RCV004376933
ClinVar Variation:
3085613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_776173.3:p.Ile593Val
CA6665364
NM_173812.5:c.1777A>G