Canonical Allele Identifier: PA2825222498
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 291333

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000634.2:p.His587Tyr
CA966587
NM_000643.2:c.1759C>T