Canonical Allele Identifier: PA915962842
Gene: GP9 HGNC NCBI

Linked Data

ClinVar Variation Id: 728112
ClinVar RCV Id: RCV000902534
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000165.1:p.Arg27His
CA2602628
NM_000174.5:c.80G>A