Canonical Allele Identifier: PA2826467971
Gene: HAL HGNC NCBI

Linked Data

ClinVar Variation Id: 310710
ClinVar RCV Id: RCV000385709 RCV003983013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245263.1:p.Val439Ile
CA6727622
NM_001258334.2:c.1315G>A