Canonical Allele Identifier: PA2826111913
Gene: LMX1B HGNC NCBI

Linked Data

ClinVar Variation Id: 379916
ClinVar RCV Id: RCV000421725
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167618.1:p.Trp76Gly
CA16605467
NM_001174147.2:c.226T>G