Canonical Allele Identifier: PA213351
Gene: RHAG HGNC NCBI

Linked Data

ClinVar Variation Id: 218296
ClinVar RCV Id: RCV000202426
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000315.2:p.Ile61Arg
CA213350
NM_000324.3:c.182T>G