Canonical Allele Identifier: PA2825232649
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 2081042
ClinVar RCV Id: RCV002993980

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000637.2:p.Glu613Asp
CA341317110
NM_000646.2:c.1839G>C
CA341317114
NM_000646.2:c.1839G>T