Canonical Allele Identifier: PA100904
Gene: EPB42 HGNC NCBI

Linked Data

ClinVar Variation Id: 132633
ClinVar RCV Id: RCV000119050
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107606.1:p.Asp145Tyr
CA345651
NM_001114134.2:c.433G>T