Canonical Allele Identifier: PA645485136
Gene: CEP41 HGNC NCBI

Linked Data

ClinVar Variation Id: 358942
ClinVar RCV Id: RCV000483238 RCV000878420 RCV001261666 RCV001702359 RCV003922590
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061188.1:p.Pro206Ala
CA4485523
NM_018718.3:c.616C>G