Canonical Allele Identifier: PA645436865
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 424906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000633.2:p.Asn1444Ser
CA967401
NM_000642.3:c.4331A>G