Canonical Allele Identifier: PA2830025866
Gene: CFAP43 HGNC NCBI

Linked Data

ClinVar Variation Id: 3143469
ClinVar RCV Id: RCV004428838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079421.5:p.Lys1132Met
CA5680311
NM_025145.7:c.3395A>T