Canonical Allele Identifier: PA100820
Gene: GP9 HGNC NCBI

Linked Data

ClinVar Variation Id: 196227
ClinVar RCV Id: RCV000177001 RCV000271819 RCV001520971
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000165.1:p.Ala156Thr
CA202222
NM_000174.5:c.466G>A