Canonical Allele Identifier: PA2825006661
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 291335
ClinVar RCV Id: RCV000314774
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000019.2:p.Tyr660Ser
CA966656
NM_000028.2:c.1979A>C