Canonical Allele Identifier: PA2826434272
Gene: CEP41 HGNC NCBI

Linked Data

ClinVar Variation Id: 30843
ClinVar RCV Id: RCV000023828 RCV001295978
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244087.1:p.Arg288Cys
CA129496
NM_001257158.2:c.862C>T