Canonical Allele Identifier: PA2828638739
Gene: EPB41 HGNC NCBI

Linked Data

ClinVar Variation Id: 2974016
ClinVar RCV Id: RCV003833590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362949.1:p.Gly173del
CA724239
NM_001376020.1:c.518_520del