Canonical Allele Identifier: PA174259
Gene: ING4 HGNC NCBI

Linked Data

ClinVar Variation Id: 161520
ClinVar RCV Id: RCV000149055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121057.1:p.Ala85Asp
CA174258
NM_001127585.2:c.254C>A