Canonical Allele Identifier: PA2826842969
Gene: HNRNPR HGNC NCBI

Linked Data

ClinVar Variation Id: 3106439
ClinVar RCV Id: RCV004399829
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284549.1:p.Thr32Ile
CA338973237
NM_001297620.2:c.95C>T