Canonical Allele Identifier: PA224421
Gene: APOH HGNC NCBI

Linked Data

ClinVar Variation Id: 96713
ClinVar RCV Id: RCV000082872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000033.2:p.Lys38Glu
CA224420
NM_000042.3:c.112A>G