Canonical Allele Identifier: PA2825232586
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 456459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000637.2:p.Phe588Val
CA966599
NM_000646.2:c.1762T>G