Allele Registry

Canonical Allele Identifier: PA100904

Gene: EPB42 HGNC NCBI

ClinVar RCV:

RCV000119050

ClinVar Variation:

132633

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107606.1:p.Asp145Tyr	CA345651 NM_001114134.2:c.433G>T