Canonical Allele Identifier: PA915963117
Gene: AGL HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000635.2:p.Thr645Ala
CA966645
NM_000644.2:c.1933A>G