Canonical Allele Identifier: PA2828109505
Gene: LHX3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2230340
ClinVar RCV Id: RCV002717551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350675.1:p.Pro313Ser
CA5330280
NM_001363746.1:c.937C>T