Canonical Allele Identifier: PA915962992
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 429532
ClinVar RCV Id: RCV000493598 RCV000667797 RCV002282176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000635.2:p.Arg343Trp
CA341343170
NM_000644.2:c.1027C>T