Canonical Allele Identifier: PA915984712
Gene: HAL HGNC NCBI

Linked Data

ClinVar Variation Id: 1691
ClinVar RCV Id: RCV000001759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245262.1:p.Pro51Leu
CA115145
NM_001258333.2:c.152C>T
CA1139532293
NM_001258333.2:c.152_153delinsTG