Allele Registry

Canonical Allele Identifier: PA1139738128

Gene: EPB41L1 HGNC NCBI

ClinVar RCV:

RCV001198025

ClinVar Variation:

931461

HGVS (amino-acid)	Matching Registered Transcripts
NP_036288.2:p.Val736Ala	CA9840213 NM_012156.2:c.2207T>C