Canonical Allele Identifier: PA2825007009
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 959928
ClinVar RCV Id: RCV001233364
ClinVar Variation Id: 1510216
ClinVar RCV Id: RCV002011599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000019.2:p.Thr1016Ser
CA341326208
NM_000028.2:c.3046A>T
CA341326214
NM_000028.2:c.3047C>G