Canonical Allele Identifier: PA2828109558
Gene: LHX3 HGNC NCBI

Linked Data

ClinVar Variation Id: 3118660
ClinVar RCV Id: RCV004415024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350675.1:p.Asp379Glu
CA5330242
NM_001363746.1:c.1137T>A
CA375518372
NM_001363746.1:c.1137T>G