Canonical Allele Identifier: PA100888
Gene: GP9 HGNC NCBI

Linked Data

ClinVar Variation Id: 13531
ClinVar RCV Id: RCV000852069 RCV001204218 RCV002222350 RCV000014486
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000165.1:p.Phe71Ser
CA123177
NM_000174.5:c.212T>C