Canonical Allele Identifier: PA645429394
Gene: ALG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 422476

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001004127.2:p.Met408Arg
CA16619817
NM_001004127.2:c.1223T>G