Canonical Allele Identifier: PA2826467870
Gene: HAL HGNC NCBI

Linked Data

ClinVar Variation Id: 310710
ClinVar RCV Id: RCV000385709 RCV003983013
JSON-LD

Amino-acid Alleles

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