Canonical Allele Identifier: PA2826467950
Gene: HAL HGNC NCBI

Linked Data

ClinVar Variation Id: 2302086
ClinVar RCV Id: RCV004154404
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245263.1:p.Val268Ala
CA6727846
NM_001258334.2:c.803T>C