Canonical Allele Identifier: PA2826112035
Gene: LMX1B HGNC NCBI

Linked Data

ClinVar Variation Id: 265491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167618.1:p.Arg261Cys
CA10588465
NM_001174147.2:c.781C>T