Canonical Allele Identifier: PA2825006583
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 291333

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000019.2:p.His587Tyr
CA966587
NM_000028.2:c.1759C>T