Canonical Allele Identifier: PA645436800
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 422206
ClinVar RCV Id: RCV000482990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000633.2:p.Phe993_Tyr994del
CA16617220
NM_000642.3:c.2977_2982del