Canonical Allele Identifier: PA915962932
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 291325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000635.2:p.Cys172Ser
CA966202
NM_000644.2:c.515G>C
CA341335241
NM_000644.2:c.514T>A