Canonical Allele Identifier: PA645436767
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 291335
ClinVar RCV Id: RCV000314774

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000633.2:p.Tyr660Ser
CA966656
NM_000642.3:c.1979A>C