Canonical Allele Identifier: PA123898
Gene: LOXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 14361

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005567.2:p.Gly153Asp
CA123897
NM_005576.4:c.458G>A