Canonical Allele Identifier: PA2826434244
Gene: CEP41 HGNC NCBI

Linked Data

ClinVar Variation Id: 358941
ClinVar RCV Id: RCV000354546 RCV001261664 RCV003430934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244087.1:p.Ala258Pro
CA4485413
NM_001257158.2:c.772G>C