Canonical Allele Identifier: PA915963225
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_000635.2:p.Met1026Thr
CA341326374
NM_000644.2:c.3077T>C