Canonical Allele Identifier: PA2828638837
Gene: EPB41 HGNC NCBI

Linked Data

ClinVar Variation Id: 1302938
ClinVar RCV Id: RCV001756437
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362950.1:p.Cys212Tyr
CA724254
NM_001376021.1:c.635G>A