Canonical Allele Identifier: PA331779
Gene: HDAC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 92043
ClinVar RCV Id: RCV000077779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159891.1:p.Thr119Met
CA331778
NM_001166419.2:c.356C>T