Canonical Allele Identifier: PA915984714
Gene: HAL HGNC NCBI

Linked Data

ClinVar Variation Id: 310715
ClinVar RCV Id: RCV000338345
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245262.1:p.Ala73Thr
CA6727836
NM_001258333.2:c.217G>A