Allele Registry

Canonical Allele Identifier: PA2826467870

Gene: HAL HGNC NCBI

ClinVar RCV:

RCV000385709

RCV003983013

ClinVar Variation:

310710

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245262.1:p.Val231Ile	CA6727622 NM_001258333.2:c.691G>A