Allele Registry

Canonical Allele Identifier: PA645485305

Gene: HAL HGNC NCBI

ClinVar RCV:

RCV000385709

RCV003983013

ClinVar Variation:

310710

HGVS (amino-acid)	Matching Registered Transcripts
NP_002099.1:p.Val439Ile	CA6727622 NM_002108.4:c.1315G>A