Canonical Allele Identifier: PA2828638976
Gene: EPB41 HGNC NCBI

Linked Data

ClinVar Variation Id: 1302938
ClinVar RCV Id: RCV001756437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362952.1:p.Cys3Tyr
CA724254
NM_001376023.1:c.8G>A