Allele Registry

Canonical Allele Identifier: PA2826467444

Gene: EPB41L1 HGNC NCBI

ClinVar RCV:

RCV001198025

ClinVar Variation:

931461

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245258.1:p.Val735Ala	CA9840213 NM_001258329.1:c.2204T>C