Canonical Allele Identifier: PA2825007017
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 642332
ClinVar RCV Id: RCV000795784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000019.2:p.Met1026Thr
CA341326374
NM_000028.2:c.3077T>C