Canonical Allele Identifier: PA2826292329
Gene: HNRNPDL HGNC NCBI

Linked Data

ClinVar Variation Id: 464386
ClinVar RCV Id: RCV000535298
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193929.1:p.Thr105Ile
CA2985060
NM_001207000.1:c.314C>T