Canonical Allele Identifier: PA122818
Gene: RNASEL HGNC NCBI

Linked Data

ClinVar Variation Id: 13006
ClinVar RCV Id: RCV000013880 RCV002279713 RCV003492293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066956.1:p.Arg462Gln
CA122817
NM_021133.4:c.1385G>A