Canonical Allele Identifier: PA2825006109
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 1062291
ClinVar RCV Id: RCV001371989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000019.2:p.Tyr106Phe
CA966134
NM_000028.2:c.317A>T