Canonical Allele Identifier: PA2741812173
Gene: GP9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2504691
ClinVar RCV Id: RCV003234282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000165.1:p.Pro50Leu
CA2602641
NM_000174.5:c.149C>T