Canonical Allele Identifier: PA2825007155
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 1107
ClinVar RCV Id: RCV000001166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000019.2:p.Arg1147Gly
CA114767
NM_000028.2:c.3439A>G