Canonical Allele Identifier: PA2828638167
Gene: EPB41 HGNC NCBI

Linked Data

ClinVar Variation Id: 811532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362943.1:p.Val214Ile
CA724256
NM_001376014.1:c.640G>A