Canonical Allele Identifier: PA645436736
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 291325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000633.2:p.Cys172Ser
CA966202
NM_000642.3:c.515G>C
CA341335241
NM_000642.3:c.514T>A