Canonical Allele Identifier: PA2741922341
Gene: LHX1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005559.2:p.His131Pro
CA399176630
NM_005568.5:c.392A>C