Canonical Allele Identifier: PA2826520838
Gene: CFAP410 HGNC NCBI

Linked Data

ClinVar Variation Id: 964390
ClinVar RCV Id: RCV001238604

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258370.1:p.Asp122His
CA410456173
NM_001271441.2:c.364G>C