Canonical Allele Identifier: PA2741814626
Gene: RHAG HGNC NCBI

Linked Data

ClinVar Variation Id: 2635235
ClinVar RCV Id: RCV003418933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000315.2:p.Ile96Thr
CA364403102
NM_000324.3:c.287T>C