Canonical Allele Identifier: PA2826111669
Gene: LMX1B HGNC NCBI

Linked Data

ClinVar Variation Id: 438683
ClinVar RCV Id: RCV000505642
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001167617.1:p.Cys59Phe
CA374909920
NM_001174146.2:c.176G>T