Canonical Allele Identifier: PA174503
Gene: CHAF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 161635
ClinVar RCV Id: RCV000149171
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005432.1:p.Thr288Ala
CA174502
NM_005441.3:c.862A>G