Canonical Allele Identifier: PA2825216932
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 2059440
ClinVar RCV Id: RCV002933731

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000633.2:p.Phe621Leu
CA341316941
NM_000642.3:c.1861T>C
CA341316961
NM_000642.3:c.1863T>G
CA341316963
NM_000642.3:c.1863T>A