Canonical Allele Identifier: PA2580105770
Gene: GP9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1915240
ClinVar RCV Id: RCV002601333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000165.1:p.Pro75Leu
CA354447553
NM_000174.5:c.224C>T