Canonical Allele Identifier: PA891855339
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 578111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000633.2:p.His1488Tyr
CA967446
NM_000642.3:c.4462C>T