Canonical Allele Identifier: PA1139675004
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 970740
ClinVar RCV Id: RCV001246369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000635.2:p.Ser440Tyr
CA966462
NM_000644.2:c.1319C>A