Canonical Allele Identifier: PA123908
Gene: LYZ HGNC NCBI

Linked Data

ClinVar Variation Id: 14376
ClinVar Variation Id: 14378

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000230.1:p.Trp82Arg
CA123906
NM_000239.3:c.244T>C
CA123912
NM_000239.3:c.244T>A