Canonical Allele Identifier: PA645511115
Gene: RHAG HGNC NCBI

Linked Data

ClinVar Variation Id: 438647
ClinVar RCV Id: RCV000505587
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000315.2:p.Leu336Ser
CA364397505
NM_000324.3:c.1007T>C