Canonical Allele Identifier: PA2825006601
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 456459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000019.2:p.Phe604Val
CA966599
NM_000028.2:c.1810T>G