Canonical Allele Identifier: PA915997362
Gene: IPO8 HGNC NCBI
ClinVar RCV:
RCV000884739
ClinVar Variation:
712730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177924.1:p.Gly811Val
CA6498478
NM_001190995.2:c.2432G>T