Canonical Allele Identifier: PA213353
Gene: RHAG HGNC NCBI

Linked Data

ClinVar Variation Id: 218295
ClinVar RCV Id: RCV000202428 RCV001781607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000315.2:p.Phe65Ser
CA213352
NM_000324.3:c.194T>C