Canonical Allele Identifier: PA645400267
Gene: LMX1B HGNC NCBI

Linked Data

ClinVar Variation Id: 379916
ClinVar RCV Id: RCV000421725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002307.2:p.Trp76Gly
CA16605467
NM_002316.4:c.226T>G