Canonical Allele Identifier: PA2499269250
Gene: CFAP410 HGNC NCBI

Linked Data

ClinVar Variation Id: 1062775
ClinVar RCV Id: RCV001372530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004919.1:p.Pro57Ser
CA410457581
NM_004928.3:c.169C>T