Canonical Allele Identifier: PA645485272
Gene: LHX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 262225
ClinVar RCV Id: RCV000242291 RCV000612505 RCV002058380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_203129.1:p.Asn328Ser
CA1272062
NM_033343.4:c.983A>G