Canonical Allele Identifier: PA2825006658
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 950117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000019.2:p.Gly659Ser
CA966655
NM_000028.2:c.1975G>A