Canonical Allele Identifier: PA2741883394
Gene: CELSR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2778469
ClinVar RCV Id: RCV003661500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001399.1:p.Asp1769Tyr
CA341501963
NM_001408.3:c.5305G>T