Canonical Allele Identifier: PA2826520225
Gene: CFAP410 HGNC NCBI

Linked Data

ClinVar Variation Id: 1062775
ClinVar RCV Id: RCV001372530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258369.1:p.Pro57Ser
CA410457581
NM_001271440.2:c.169C>T