Canonical Allele Identifier: PA915963101
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 291333
ClinVar RCV Id: RCV000335847 RCV002519359 RCV001567373
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000635.2:p.His587Tyr
CA966587
NM_000644.2:c.1759C>T