Canonical Allele Identifier: PA2825221779
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 2147221
ClinVar RCV Id: RCV003077078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000634.2:p.Val404Ala
CA966429
NM_000643.2:c.1211T>C