Canonical Allele Identifier: PA2829659476
Gene: IPO8 HGNC NCBI
ClinVar RCV:
RCV000884739
ClinVar Variation:
712730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006381.2:p.Gly1016Val
CA6498478
NM_006390.4:c.3047G>T