Canonical Allele Identifier: PA2826881949
Gene: CEP97 HGNC NCBI

Linked Data

ClinVar Variation Id: 2876531
ClinVar RCV Id: RCV003710335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290330.1:p.Asn439His
CA353877707
NM_001303401.2:c.1315A>C