Canonical Allele Identifier: PA645511114
Gene: RHAG HGNC NCBI

Linked Data

ClinVar Variation Id: 438646
ClinVar RCV Id: RCV000505544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000315.2:p.Ile149Met
CA364401417
NM_000324.3:c.447T>G