Canonical Allele Identifier: PA645436757
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 256719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000633.2:p.Lys385Asn
CA966399
NM_000642.3:c.1155G>T
CA341344830
NM_000642.3:c.1155G>C