Canonical Allele Identifier: PA249964
Gene: CHAF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 183350
ClinVar RCV Id: RCV000162182
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005432.1:p.Ile166Val
CA249963
NM_005441.3:c.496A>G