Canonical Allele Identifier: PA2826843012
Gene: HNRNPR HGNC NCBI

Linked Data

ClinVar Variation Id: 2634546
ClinVar RCV Id: RCV003392823
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284550.1:p.Pro443Leu
CA339258363
NM_001297621.2:c.1328C>T