Canonical Allele Identifier: PA2826434262
Gene: CEP41 HGNC NCBI

Linked Data

ClinVar Variation Id: 957287
ClinVar RCV Id: RCV001230240
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244087.1:p.Gly280Ser
CA4485396
NM_001257158.2:c.838G>A