Canonical Allele Identifier: PA645436742
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 265986
ClinVar RCV Id: RCV000256372

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000633.2:p.Ser258Pro
CA10588921
NM_000642.3:c.772T>C