Canonical Allele Identifier: PA2826015993
Gene: EPB41 HGNC NCBI

Linked Data

ClinVar Variation Id: 811532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159478.1:p.Val214Ile
CA724256
NM_001166006.2:c.640G>A