Canonical Allele Identifier: PA2828109487
Gene: LHX3 HGNC NCBI

Linked Data

ClinVar Variation Id: 279837
ClinVar RCV Id: RCV000302742 RCV000766051 RCV001273808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350675.1:p.Arg296Pro
CA5330291
NM_001363746.1:c.887G>C