Canonical Allele Identifier: PA2573207879
Gene: CELSR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1367036
ClinVar RCV Id: RCV001962215
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001399.1:p.Asn1800Ile
CA987537
NM_001408.3:c.5399A>T