Canonical Allele Identifier: PA2828639281
Gene: EPB41 HGNC NCBI

Linked Data

ClinVar Variation Id: 811532
ClinVar RCV Id: RCV001001476 RCV002068772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362956.1:p.Val5Ile
CA724256
NM_001376027.1:c.13G>A